FDA 510(k)

INTERCEPTRE LAPAROSCOPIC INSTRUMENTS

K-Number: K974592 · 1998-01-12

Decision Date1998-01-12

Product CodeGCJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

INTERCEPTRE LAPAROSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1998-01-12 under 510(k) number K974592. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERCEPTRE LAPAROSCOPIC INSTRUMENTS?

INTERCEPTRE LAPAROSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1998-01-12. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K974592.

When did INTERCEPTRE LAPAROSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

INTERCEPTRE LAPAROSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1998-01-12, under 510(k) number K974592.

Who is the listed applicant for INTERCEPTRE LAPAROSCOPIC INSTRUMENTS?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERCEPTRE LAPAROSCOPIC INSTRUMENTS?

The FDA product code for INTERCEPTRE LAPAROSCOPIC INSTRUMENTS is GCJ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.