Cleared Traditional

K920205 - OTT INSUFFLATION FILTER TUBING

K920205 is an FDA 510(k) clearance for OTT INSUFFLATION FILTER TUBING, manufactured by Georgia Biomedical Research Group, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HIF cleared through the Traditional 510(k) pathway after a 648-day FDA review.

K920205 · Georgia Biomedical Research Group, Inc. · Obstetrics & Gynecology device
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Oct 1993
Decision
648d
Days
Class 2
Risk

K920205 is an FDA 510(k) clearance for the OTT INSUFFLATION FILTER TUBING. Classified as Insufflator, Laparoscopic (product code HIF), Class II - Special Controls.

Submitted by Georgia Biomedical Research Group, Inc. (Macon, US). The FDA issued a Cleared decision on October 25, 1993 after a review of 648 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.1730 - the FDA obstetrics and gynecology 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Obstetrics & Gynecology submissions.

View all Georgia Biomedical Research Group, Inc. devices

FDA 510(k) Submission Details - K920205

510(k) Number K920205 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 1992
Decision Date October 25, 1993
Days to Decision 648 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
488d slower than avg
Panel avg: 160d · This submission: 648d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HIF Device Classification - Class 2, Special Controls

Product Code HIF Insufflator, Laparoscopic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.1730
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 Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HIF Insufflator, Laparoscopic

All 133
Devices cleared under the same product code (HIF) and FDA review panel - the closest regulatory comparables to K920205.
DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING
K934131 · Deroyal Industries, Inc. · Mar 1994
DAVOL LAPAROSCOPIC INSUFFLATION TUBING SET
K935503 · Davol, Inc. · Mar 1994
INFILTUBE
K925558 · Medsurg Industries, Inc. · Mar 1994
INSUFFLATOR CONNECTING FILTER
K923194 · Procedure Products, Inc. · Oct 1993
INSUFFLATOR TUBING/FILTER KIT
K922244 · O.R. Concepts, Inc. · Sep 1993
MEDICAM 900 INSUFFLATOR WITH ACCESSORIES
K921837 · Kirschner Medical Corp. · Feb 1993