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FDA 510(k)

MEDSCOPE 8MM AND 10MM LAPAROSCOPE

K-Number: K903663 · 1992-02-11

Decision Date1992-02-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDSCOPE 8MM AND 10MM LAPAROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Medscope Corp.. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K903663. 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 MEDSCOPE 8MM AND 10MM LAPAROSCOPE?

MEDSCOPE 8MM AND 10MM LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Medscope Corp.. The 510(k) number is K903663.

When did MEDSCOPE 8MM AND 10MM LAPAROSCOPE receive FDA 510(k) clearance?

MEDSCOPE 8MM AND 10MM LAPAROSCOPE received FDA 510(k) clearance on 1992-02-11, under 510(k) number K903663.

Who is the listed applicant for MEDSCOPE 8MM AND 10MM LAPAROSCOPE?

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

What is the FDA product code for MEDSCOPE 8MM AND 10MM LAPAROSCOPE?

The FDA product code for MEDSCOPE 8MM AND 10MM LAPAROSCOPE is HET.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medscope Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: HET)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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