Cleared Traditional

K902722 - BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM

K902722 is the FDA 510(k) clearance for BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM by Davol, Inc.. It is a Class 2 Obstetrics & Gynecology device (product code HET) cleared through the Traditional 510(k) pathway after a 149-day FDA review.

K902722 · Davol, Inc. · Obstetrics & Gynecology device
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Nov 1990
Decision
149d
Days
Class 2
Risk

K902722 is an FDA 510(k) clearance for the BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM. Classified as Laparoscope, Gynecologic (and Accessories) (product code HET), Class II - Special Controls.

Submitted by Davol, Inc. (Cranston, US). The FDA issued a Cleared decision on November 16, 1990 after a review of 149 days - within the typical 510(k) review window.

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: 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 Davol, Inc. devices

Submission Details

510(k) Number K902722 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 20, 1990
Decision Date November 16, 1990
Days to Decision 149 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
11d faster than avg
Panel avg: 160d · This submission: 149d
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 K902722.
V. MUELLER TROCARS/TROCAR SLEEVES & NEEDLES
K904143 · Baxter Healthcare Corp · Dec 1990
ENDOPATH UNSHIELDED DISPOSABLE SURGICAL TROCAR
K904104 · Ethicon, Inc. · Dec 1990
GRASPING FORCEPS/ALIGATOR FORCEPS/NEEDLE HOLDERS
K904142 · Baxter Healthcare Corp · Dec 1990
AUTO SUTURE LAPAROSCOPY ACCESSORY KIT
K903780 · United States Surgical, A Division of Tyco Healthc · Oct 1990
AUTO SUTURE(R) ENDOSCOPIC SCISSORS
K903206 · United States Surgical, A Division of Tyco Healthc · Oct 1990
LAPAROSCOPIC ACCESS SHEATH SET
K903124 · Cook, Inc. · Oct 1990