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FDA 510(k)

COOLEY ANGLED SCISSOR - 1MM PROBE POINT

K-Number: K760791 · 1976-11-11

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-11-11
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COOLEY ANGLED SCISSOR - 1MM PROBE POINT is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-11-11 under 510(k) number K760791. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOLEY ANGLED SCISSOR - 1MM PROBE POINT?

COOLEY ANGLED SCISSOR - 1MM PROBE POINT is a medical device that received FDA 510(k) clearance on 1976-11-11. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760791.

When did COOLEY ANGLED SCISSOR - 1MM PROBE POINT receive FDA 510(k) clearance?

COOLEY ANGLED SCISSOR - 1MM PROBE POINT received FDA 510(k) clearance on 1976-11-11, under 510(k) number K760791.

Who is the listed applicant for COOLEY ANGLED SCISSOR - 1MM PROBE POINT?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COOLEY ANGLED SCISSOR - 1MM PROBE POINT?

The FDA product code for COOLEY ANGLED SCISSOR - 1MM PROBE POINT is DWS.

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Related Devices (Code: DWS)

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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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