Cleared Traditional

K760612 - SPACELABS SERIES 1000

K760612 is an FDA 510(k) clearance for SPACELABS SERIES 1000, manufactured by Spacelabs, Inc.. The device is a Class 2 Cardiovascular device with product code DPS cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K760612 · Spacelabs, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1976
Decision
11d
Days
Class 2
Risk

K760612 is an FDA 510(k) clearance for the SPACELABS SERIES 1000. Classified as Electrocardiograph (product code DPS), Class II - Special Controls.

Submitted by Spacelabs, Inc. (Mchenry, US). The FDA issued a Cleared decision on September 21, 1976 after a review of 11 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2340 - the FDA cardiovascular device 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 Spacelabs, Inc. devices

FDA 510(k) Submission Details - K760612

510(k) Number K760612 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 1976
Decision Date September 21, 1976
Days to Decision 11 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
114d faster than avg
Panel avg: 125d · This submission: 11d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DPS Device Classification - Class 2, Special Controls

Product Code DPS Electrocardiograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2340
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DPS Electrocardiograph

All 279
Devices cleared under the same product code (DPS) and FDA review panel - the closest regulatory comparables to K760612.
THREE-CHANNEL STRESS TEST SYSTEM (M633)
K760854 · Quinton, Inc. · Nov 1976
MONITOR, ELECTROCARDIOSCOPE
K760266 · Burdick Corp. · Oct 1976
LIFEPAK 5 CARDIOSCOPE MODULE (NPN 5)
K760677 · Physio-Control Corp. · Oct 1976
ELECTROCARDIOGRAPH (#1505A)
K760542 · Hewlett-Packard Co. · Sep 1976
STRESS SYSTEM, SINGLE-CHANNEL (#21125)
K760463 · Hewlett-Packard Co. · Aug 1976
STRESS SYSTEM, 3-CHANNEL (#21127A)
K760465 · Hewlett-Packard Co. · Aug 1976