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FDA 510(k)

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)

K-Number: K760452 · 1976-08-30

ApplicantAmerican Cystocope Makers, Inc.
Decision Date1976-08-30
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92) is the device name listed in this FDA 510(k) record. The listed applicant is American Cystocope Makers, Inc.. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760452. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)?

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92) is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is American Cystocope Makers, Inc.. The 510(k) number is K760452.

When did COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92) receive FDA 510(k) clearance?

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92) received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760452.

Who is the listed applicant for COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)?

The FDA 510(k) record lists American Cystocope Makers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)?

The FDA product code for COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92) is FDF.

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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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