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FDA 510(k)

CONTACT-MICRO COLPOHYSTEROSCOPE

K-Number: K810569 · 1981-07-16

Decision Date1981-07-16
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONTACT-MICRO COLPOHYSTEROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1981-07-16 under 510(k) number K810569. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTACT-MICRO COLPOHYSTEROSCOPE?

CONTACT-MICRO COLPOHYSTEROSCOPE is a medical device that received FDA 510(k) clearance on 1981-07-16. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K810569.

When did CONTACT-MICRO COLPOHYSTEROSCOPE receive FDA 510(k) clearance?

CONTACT-MICRO COLPOHYSTEROSCOPE received FDA 510(k) clearance on 1981-07-16, under 510(k) number K810569.

Who is the listed applicant for CONTACT-MICRO COLPOHYSTEROSCOPE?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTACT-MICRO COLPOHYSTEROSCOPE?

The FDA product code for CONTACT-MICRO COLPOHYSTEROSCOPE is HIH.

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 KARL STORZ Endoscopy-America, Inc. 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.

View all 355 devices →

Related Devices (Code: HIH)

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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