Cleared Traditional

K914997 - ASP-IRRATOR

K914997 is an FDA 510(k) clearance for ASP-IRRATOR, manufactured by Conmedcorp. The device is a Class 2 General & Plastic Surgery device with product code GCJ cleared through the Traditional 510(k) pathway after a 61-day FDA review.

K914997 · Conmedcorp · General & Plastic Surgery device
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Jan 1992
Decision
61d
Days
Class 2
Risk

K914997 is an FDA 510(k) clearance for the ASP-IRRATOR. Classified as Laparoscope, General & Plastic Surgery (product code GCJ), Class II - Special Controls.

Submitted by Conmedcorp (Utica, US). The FDA issued a Cleared decision on January 7, 1992 after a review of 61 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 876.1500 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

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FDA 510(k) Submission Details - K914997

510(k) Number K914997 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 1991
Decision Date January 07, 1992
Days to Decision 61 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
54d faster than avg
Panel avg: 115d · This submission: 61d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GCJ Device Classification - Class 2, Special Controls

Product Code GCJ Laparoscope, General & Plastic Surgery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GCJ Laparoscope, General & Plastic Surgery

All 803
Devices cleared under the same product code (GCJ) and FDA review panel - the closest regulatory comparables to K914997.
MARLOW LAPAROSCOPIC SCISSORS
K914869 · Marlo Surgical Technology · Jan 1992
ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR
K915239 · Ethicon, Inc. · Jan 1992
SMITH & NEPHEW DYONICS LAPAROSCOPY SYSTEM
K914919 · Smith & Nephew Dyonics, Inc. · Jan 1992
MARLOW/REDDICK LAPAROSCOPIC NEEDLE HOLDERS
K913954 · Marlo Surgical Technology · Dec 1991
SUCTION/IRRIGATION KITTNER
K914781 · O.R. Concepts, Inc. · Dec 1991
SUCTION/IRRIGATION PROBE
K914782 · O.R. Concepts, Inc. · Dec 1991