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FDA 510(k)

MONOSCOPY(TM) BRAND, TROCAR REDUCER SET

K-Number: K902563 · 1990-09-04

ApplicantDexide, Inc.
Decision Date1990-09-04
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MONOSCOPY(TM) BRAND, TROCAR REDUCER SET is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1990-09-04 under 510(k) number K902563. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOSCOPY(TM) BRAND, TROCAR REDUCER SET?

MONOSCOPY(TM) BRAND, TROCAR REDUCER SET is a medical device that received FDA 510(k) clearance on 1990-09-04. The listed applicant is Dexide, Inc.. The 510(k) number is K902563.

When did MONOSCOPY(TM) BRAND, TROCAR REDUCER SET receive FDA 510(k) clearance?

MONOSCOPY(TM) BRAND, TROCAR REDUCER SET received FDA 510(k) clearance on 1990-09-04, under 510(k) number K902563.

Who is the listed applicant for MONOSCOPY(TM) BRAND, TROCAR REDUCER SET?

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(TM) BRAND, TROCAR REDUCER SET?

The FDA product code for MONOSCOPY(TM) BRAND, TROCAR REDUCER SET is HET.

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Other records listing Dexide, Inc. as applicant

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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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