Cleared Traditional

K882436 - LASER - 1000

K882436 is an FDA 510(k) clearance for LASER - 1000, manufactured by Panoramic Corp.. The device is a Class 2 Radiology device with product code EHD cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K882436 · Panoramic Corp. · Radiology device
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Aug 1988
Decision
51d
Days
Class 2
Risk

K882436 is an FDA 510(k) clearance for the LASER - 1000. Classified as Unit, X-ray, Extraoral With Timer (product code EHD), Class II - Special Controls.

Submitted by Panoramic Corp. (Ft. Wayne, US). The FDA issued a Cleared decision on August 4, 1988 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - 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.

FDA 510(k) Submission Details - K882436

510(k) Number K882436 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 14, 1988
Decision Date August 04, 1988
Days to Decision 51 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 107d · This submission: 51d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EHD Device Classification - Class 2, Special Controls

Product Code EHD Unit, X-ray, Extraoral With Timer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - EHD Unit, X-ray, Extraoral With Timer

All 190
Devices cleared under the same product code (EHD) and FDA review panel - the closest regulatory comparables to K882436.
COFFMAN TOMOGRAPH
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K895467 · Siemens Medical Solutions USA, Inc. · Nov 1989
PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE
K875212 · Kevex Corp. · Jun 1988
AXIAL TOME, 60, FLUORO AND TOMAX
K872825 · Axialtome Corp. · Mar 1988
MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY
K874238 · Belmont Equipment Corp. · Dec 1987
K882436 · LASER - 1000
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