Cleared Traditional

K932276 - CO2 HYDROMAT PUMP FOR IRRIGATION

K932276 is the FDA 510(k) clearance for CO2 HYDROMAT PUMP FOR IRRIGATION by KARL STORZ Endoscopy-America, Inc.. It is a Class 2 Obstetrics & Gynecology device (product code HET) cleared through the Traditional 510(k) pathway after a 657-day FDA review.

K932276 · KARL STORZ Endoscopy-America, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1995
Decision
657d
Days
Class 2
Risk

K932276 is an FDA 510(k) clearance for the CO2 HYDROMAT PUMP FOR IRRIGATION, MODEL #26310020. Classified as Laparoscope, Gynecologic (and Accessories) (product code HET), Class II - Special Controls.

Submitted by KARL STORZ Endoscopy-America, Inc. (Kennesaw, US). The FDA issued a Cleared decision on February 28, 1995 after a review of 657 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.1720 - 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 KARL STORZ Endoscopy-America, Inc. devices

Submission Details

510(k) Number K932276 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 12, 1993
Decision Date February 28, 1995
Days to Decision 657 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
497d slower than avg
Panel avg: 160d · This submission: 657d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HET Laparoscope, Gynecologic (and Accessories)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.1720
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 - HET Laparoscope, Gynecologic (and Accessories)

All 150
Devices cleared under the same product code (HET) and FDA review panel - the closest regulatory comparables to K932276.
AESCULAP LAPAROSCOPIC ANCILLARY DEVICES
K943603 · Aesculap, Inc. · Mar 1995
KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER
K945982 · KARL STORZ Endoscopy-America, Inc. · Mar 1995
LAPAROSCOPE AND ACCESSORIES FOR OB/GYN
K950232 · Olympus America, Inc. · Mar 1995
TROCAR AND CANNULA ACCESSORY
K945741 · Applied Medical Resources · Feb 1995
CONMED 7/8MM GASKET REDUCER FOR USE WITH TROGARD(TM) TROCAR SLEEVE
K946235 · Conmedcorp · Feb 1995
KARL STORZ SUCTION/IRRIGATION TUBES, CANNULAE
K945100 · KARL STORZ Endoscopy-America, Inc. · Jan 1995