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FDA 510(k)

P-S SUCTION RESERVIOR

K-Number: K820474 · 1982-03-08

ApplicantPudenz-Schulte Medical Research Corp.
Decision Date1982-03-08
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

P-S SUCTION RESERVIOR 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 1982-03-08 under 510(k) number K820474. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P-S SUCTION RESERVIOR?

P-S SUCTION RESERVIOR is a medical device that received FDA 510(k) clearance on 1982-03-08. The listed applicant is Pudenz-Schulte Medical Research Corp.. The 510(k) number is K820474.

When did P-S SUCTION RESERVIOR receive FDA 510(k) clearance?

P-S SUCTION RESERVIOR received FDA 510(k) clearance on 1982-03-08, under 510(k) number K820474.

Who is the listed applicant for P-S SUCTION RESERVIOR?

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 SUCTION RESERVIOR?

The FDA product code for P-S SUCTION RESERVIOR is GCY.

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Related Devices (Code: GCY)

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.

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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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