Cleared Traditional

DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032E (K942043) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K942043 · Alm Surgical Equipment, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1994
Decision
76d
Days
Class 1
Risk

K942043 is an FDA 510(k) clearance for the DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032E. Classified as Table, Operating-room, Ac-powered (product code FQO), Class I - General Controls.

Submitted by Alm Surgical Equipment, Inc. (Anaheim, US). The FDA issued a Cleared decision on July 13, 1994 after a review of 76 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4960 - the FDA general and plastic surgery device 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 Alm Surgical Equipment, Inc. devices

Submission Details

510(k) Number K942043 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 28, 1994
Decision Date July 13, 1994
Days to Decision 76 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
39d faster than avg
Panel avg: 115d · This submission: 76d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FQO Table, Operating-room, Ac-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4960
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.