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FDA 510(k)

P-S MEDICAL BERLIN VISADUCT KIT

K-Number: K832677 · 1983-12-08

ApplicantPudenz-Schulte Medical Research Corp.
Decision Date1983-12-08
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

P-S MEDICAL BERLIN VISADUCT KIT 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 1983-12-08 under 510(k) number K832677. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P-S MEDICAL BERLIN VISADUCT KIT?

P-S MEDICAL BERLIN VISADUCT KIT is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Pudenz-Schulte Medical Research Corp.. The 510(k) number is K832677.

When did P-S MEDICAL BERLIN VISADUCT KIT receive FDA 510(k) clearance?

P-S MEDICAL BERLIN VISADUCT KIT received FDA 510(k) clearance on 1983-12-08, under 510(k) number K832677.

Who is the listed applicant for P-S MEDICAL BERLIN VISADUCT KIT?

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 MEDICAL BERLIN VISADUCT KIT?

The FDA product code for P-S MEDICAL BERLIN VISADUCT KIT is KOA.

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Other records listing Pudenz-Schulte Medical Research Corp. as applicant

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Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, 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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