Cleared Traditional

K920310 - SIENET ARCHIVE SERVER

K920310 is an FDA 510(k) clearance for SIENET ARCHIVE SERVER, manufactured by Siemens Gammasonics, Inc.. The device is a Class 1 Radiology device with product code LMD cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K920310 · Siemens Gammasonics, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1992
Decision
67d
Days
Class 1
Risk

K920310 is an FDA 510(k) clearance for the SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE. Classified as System, Digital Image Communications, Radiological (product code LMD), Class I - General Controls.

Submitted by Siemens Gammasonics, Inc. (Hoffman Estates, US). The FDA issued a Cleared decision on March 30, 1992 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2020 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Siemens Gammasonics, Inc. devices

FDA 510(k) Submission Details - K920310

510(k) Number K920310 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 23, 1992
Decision Date March 30, 1992
Days to Decision 67 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 107d · This submission: 67d
Pathway characteristics
Predicate-based equivalence.

LMD Device Classification - Class 1, General Controls

Product Code LMD System, Digital Image Communications, Radiological
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.2020
Definition A Medical Image Communications Device Provides Electronic Transfer Of Medical Image Data Between Medical Devices. It May Include A Physical Communications Medium, Modems, Interfaces, And A Communications Protocol. It May Provide Simple Image Review Software Functionality For Medical Image Processing And Manipulation, Such As Grayscale Window And Level, Zoom And Pan, User Delineated Geometric Measurements, Compression, Or User Added Image Annotations. The Device Does Not Perform Advanced Image Processing Or Complex Quantitative Functions.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - LMD System, Digital Image Communications, Radiological

All 28
Devices cleared under the same product code (LMD) and FDA review panel - the closest regulatory comparables to K920310.
KODAK EKTASCAN IMAGELINK SYSTEM (KEIS)
K931551 · Eastman Kodak Company · Jun 1993
SIENET CAMERA SERVER
K923582 · Siemens Gammasonics, Inc. · Oct 1992
3M DIGITAL DISK INTERFACE UNIT
K920268 · 3M Company · May 1992
PHILIPS TELESCAN
K911773 · Philips Medical Systems, Inc. · Jun 1991
KODAK EKTASCAN DIGITAL INTERFACE/FOR AT&T
K911405 · Eastman Kodak Company · Apr 1991
PACSNET RESEARCH TOOLKIT
K905199 · Siemens Gammasonics, Inc. · Jan 1991