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FDA 510(k)

INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT

K-Number: K932692 · 1993-12-27

ApplicantInnerdyne Medical, Inc.
Decision Date1993-12-27
Product CodeGCJ
Advisory CommitteeGU
DecisionUnknown

Device Summary

INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Innerdyne Medical, Inc.. It received FDA 510(k) clearance on 1993-12-27 under 510(k) number K932692. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT?

INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT is a medical device that received FDA 510(k) clearance on 1993-12-27. The listed applicant is Innerdyne Medical, Inc.. The 510(k) number is K932692.

When did INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT receive FDA 510(k) clearance?

INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT received FDA 510(k) clearance on 1993-12-27, under 510(k) number K932692.

Who is the listed applicant for INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT?

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

What is the FDA product code for INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT?

The FDA product code for INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT is GCJ.

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Related Devices (Code: 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.

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