Cleared Traditional

K900808 - RAPID AUTOMATIC PNEUMOPERITONEUM-I

K900808 is the FDA 510(k) clearance for RAPID AUTOMATIC PNEUMOPERITONEUM-I by Trek Medical Products, Inc.. It is a Class 2 Obstetrics & Gynecology device (product code HIF) cleared through the Traditional 510(k) pathway after a 210-day FDA review.

K900808 · Trek Medical Products, Inc. · Obstetrics & Gynecology device
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Sep 1990
Decision
210d
Days
Class 2
Risk

K900808 is an FDA 510(k) clearance for the RAPID AUTOMATIC PNEUMOPERITONEUM-I. Classified as Insufflator, Laparoscopic (product code HIF), Class II - Special Controls.

Submitted by Trek Medical Products, Inc. (Muckwonago, US). The FDA issued a Cleared decision on September 19, 1990 after a review of 210 days - an extended review cycle.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Trek Medical Products, Inc. devices

Submission Details

510(k) Number K900808 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 21, 1990
Decision Date September 19, 1990
Days to Decision 210 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
50d slower than avg
Panel avg: 160d · This submission: 210d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 55
Devices cleared under the same product code (HIF) and FDA review panel - the closest regulatory comparables to K900808.
DEROYAL SURGICAL DISPOSABLE INSUFFLATION TUBING
K934131 · Deroyal Industries, Inc. · Mar 1994
MEDICAM 900 INSUFFLATOR WITH ACCESSORIES
K921837 · Kirschner Medical Corp. · Feb 1993
LAPAROSCOPIC INSUFLATION Y TUBING
K911479 · United States Endoscopy Group, Inc. · Apr 1991
ELECTRONIC INSUFFLATOR, MODEL NO. 2054.60
K882185 · Richard Wolf Medical Instruments Corp. · Jun 1988
CARBON DIOXIDE INSUFFLATOR/LAPARO & HI FLOW LASER/
K871928 · Medline Industries, Inc. · Nov 1987
MEDICAL DYNAMICS MCCONNELL PRECISION ELEC-INSUFFLA
K845021 · Medline Industries, Inc. · May 1985