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FDA 510(k)

MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED

K-Number: K912980 · 1991-07-26

ApplicantDexide, Inc.
Decision Date1991-07-26
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K912980. 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 MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED?

MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Dexide, Inc.. The 510(k) number is K912980.

When did MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED receive FDA 510(k) clearance?

MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED received FDA 510(k) clearance on 1991-07-26, under 510(k) number K912980.

Who is the listed applicant for MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED?

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 MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED?

The FDA product code for MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED is GCJ.

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Other records listing Dexide, Inc. as applicant

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Related Devices (Code: GCJ)

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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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