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FDA 510(k)

POLLACK CHAIN CYSOURETHROGRAM SET

K-Number: K810370 · 1981-03-20

ApplicantVance Products, Inc.
Decision Date1981-03-20
Product CodeFGI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

POLLACK CHAIN CYSOURETHROGRAM SET is the device name listed in this FDA 510(k) record. The listed applicant is Vance Products, Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810370. The device is classified under product code FGI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLLACK CHAIN CYSOURETHROGRAM SET?

POLLACK CHAIN CYSOURETHROGRAM SET is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Vance Products, Inc.. The 510(k) number is K810370.

When did POLLACK CHAIN CYSOURETHROGRAM SET receive FDA 510(k) clearance?

POLLACK CHAIN CYSOURETHROGRAM SET received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810370.

Who is the listed applicant for POLLACK CHAIN CYSOURETHROGRAM SET?

The FDA 510(k) record lists Vance Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POLLACK CHAIN CYSOURETHROGRAM SET?

The FDA product code for POLLACK CHAIN CYSOURETHROGRAM SET is FGI.

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Other records listing Vance Products, Inc. as applicant

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.

K820313VPI-FAIR URETHRAL STENTK812995VANCE-JACOBELLIS MICROHEMATURIA CATHETERK813278VPI URETERAL DILATATION BALLON CATHETERK812785VANCE-AMBROSE RESECTOSCOPE FORCEPSK812057VANCE CYSTOSCOPICK811833VNACE FASCIAL DILATOR SET

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Related Devices (Code: FGI)

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.

K023019VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000Vomed Volzer Medizintechnik GmbH & Co.K013360DFINER UROLOGICAL CATHETERNeoseed Technology,Llc

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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