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FDA 510(k)

P-S BERLIN VESSEL CLAMP

K-Number: K820949 · 1982-04-29

ApplicantPudenz-Schulte Medical Research Corp.
Decision Date1982-04-29
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

P-S BERLIN VESSEL CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Pudenz-Schulte Medical Research Corp.. It received FDA 510(k) clearance on 1982-04-29 under 510(k) number K820949. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P-S BERLIN VESSEL CLAMP?

P-S BERLIN VESSEL CLAMP is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Pudenz-Schulte Medical Research Corp.. The 510(k) number is K820949.

When did P-S BERLIN VESSEL CLAMP receive FDA 510(k) clearance?

P-S BERLIN VESSEL CLAMP received FDA 510(k) clearance on 1982-04-29, under 510(k) number K820949.

Who is the listed applicant for P-S BERLIN VESSEL CLAMP?

The FDA 510(k) record lists Pudenz-Schulte Medical Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P-S BERLIN VESSEL CLAMP?

The FDA product code for P-S BERLIN VESSEL CLAMP is DXC.

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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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