Cleared Traditional

K780720 - IDENTI-LOOPS

K780720 is an FDA 510(k) clearance for IDENTI-LOOPS, manufactured by Berkeley Bio-Medical, Inc.. The device is a Class 1 General & Plastic Surgery device with product code GAD cleared through the Traditional 510(k) pathway after a 169-day FDA review.

K780720 · Berkeley Bio-Medical, Inc. · General & Plastic Surgery device
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Oct 1978
Decision
169d
Days
Class 1
Risk

K780720 is an FDA 510(k) clearance for the IDENTI-LOOPS. Classified as Retractor (product code GAD), Class I - General Controls.

Submitted by Berkeley Bio-Medical, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 17, 1978 after a review of 169 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Berkeley Bio-Medical, Inc. devices

FDA 510(k) Submission Details - K780720

510(k) Number K780720 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 01, 1978
Decision Date October 17, 1978
Days to Decision 169 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
54d slower than avg
Panel avg: 115d · This submission: 169d
Pathway characteristics
Predicate-based equivalence.

GAD Device Classification - Class 1, General Controls

Product Code GAD Retractor
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
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 - GAD Retractor

All 62
Devices cleared under the same product code (GAD) and FDA review panel - the closest regulatory comparables to K780720.
DEEP BALFOUR BLADE FOR WILKINSON RETRACT
K801611 · Edward Weck, Inc. · Aug 1980
SPREADER
K781445 · Orthopedic Equipment Co., Inc. · Sep 1979
TISSURE RETRACTORS
K791122 · Xomed, Inc. · Jul 1979
ULTRASOUND IMAGING SYSTEM
K780993 · Boehringer Mannheim Corp. · Aug 1978
NEIVS TRACHEOTOMY RETRACTOR
K772378 · Edward Weck, Inc. · Mar 1978
HEISS RETRACTOR
K771191 · Edward Weck, Inc. · Jul 1977