FDA 510(k)

WALTHER CATHETERS, MALE, FEMALE

K-Number: K926369 · 1993-05-21

Decision Date1993-05-21

Product CodeGBM

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

WALTHER CATHETERS, MALE, FEMALE is the device name listed in this FDA 510(k) record. The listed applicant is Thomasville Medical Assoc.. It received FDA 510(k) clearance on 1993-05-21 under 510(k) number K926369. The device is classified under product code GBM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALTHER CATHETERS, MALE, FEMALE?

WALTHER CATHETERS, MALE, FEMALE is a medical device that received FDA 510(k) clearance on 1993-05-21. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K926369.

When did WALTHER CATHETERS, MALE, FEMALE receive FDA 510(k) clearance?

WALTHER CATHETERS, MALE, FEMALE received FDA 510(k) clearance on 1993-05-21, under 510(k) number K926369.

Who is the listed applicant for WALTHER CATHETERS, MALE, FEMALE?

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

What is the FDA product code for WALTHER CATHETERS, MALE, FEMALE?

The FDA product code for WALTHER CATHETERS, MALE, FEMALE is GBM.

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Other records listing Thomasville Medical Assoc. 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.