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FDA 510(k)

PROCTOSCOPE #501

K-Number: K790856 · 1979-05-29

ApplicantC. Intl.
Decision Date1979-05-29
Product CodeGCF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PROCTOSCOPE #501 is the device name listed in this FDA 510(k) record. The listed applicant is C. Intl.. It received FDA 510(k) clearance on 1979-05-29 under 510(k) number K790856. The device is classified under product code GCF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCTOSCOPE #501?

PROCTOSCOPE #501 is a medical device that received FDA 510(k) clearance on 1979-05-29. The listed applicant is C. Intl.. The 510(k) number is K790856.

When did PROCTOSCOPE #501 receive FDA 510(k) clearance?

PROCTOSCOPE #501 received FDA 510(k) clearance on 1979-05-29, under 510(k) number K790856.

Who is the listed applicant for PROCTOSCOPE #501?

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

What is the FDA product code for PROCTOSCOPE #501?

The FDA product code for PROCTOSCOPE #501 is GCF.

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.

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Other records listing C. Intl. 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.

K792494CATHETERIZATION FORCEPK790855SURGICAL DRAPE CLIP #201K790853EASY-SPECK790852VAGI-SPECK790851VAGI-PRESS #401K790854FORCEPS #101 AND #102

View all 7 devices →

Related Devices (Code: GCF)

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.

K945209PROCTOSCOPEA & ACCESSORIES, SIGMOIDOSCOPES & ACCESSORIES, PROCTOLOGY INSTRUMENTSKARL STORZ Endoscopy-America, Inc.

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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