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FDA 510(k)

DEXIDE LAPAROSCOPIC ACCESSORIES

K-Number: K923845 · 1992-11-25

ApplicantDexide, Inc.
Decision Date1992-11-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEXIDE LAPAROSCOPIC ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1992-11-25 under 510(k) number K923845. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXIDE LAPAROSCOPIC ACCESSORIES?

DEXIDE LAPAROSCOPIC ACCESSORIES is a medical device that received FDA 510(k) clearance on 1992-11-25. The listed applicant is Dexide, Inc.. The 510(k) number is K923845.

When did DEXIDE LAPAROSCOPIC ACCESSORIES receive FDA 510(k) clearance?

DEXIDE LAPAROSCOPIC ACCESSORIES received FDA 510(k) clearance on 1992-11-25, under 510(k) number K923845.

Who is the listed applicant for DEXIDE LAPAROSCOPIC ACCESSORIES?

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

What is the FDA product code for DEXIDE LAPAROSCOPIC ACCESSORIES?

The FDA product code for DEXIDE LAPAROSCOPIC ACCESSORIES is GEI.

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Other records listing Dexide, Inc. as applicant

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Related Devices (Code: GEI)

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Official Source

View on FDA Database →

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

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