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FDA 510(k)

VANCE CYSTOSCOPIC

K-Number: K812057 · 1981-07-31

ApplicantVance Products, Inc.
Decision Date1981-07-31
Product CodeFBK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VANCE CYSTOSCOPIC 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 1981-07-31 under 510(k) number K812057. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANCE CYSTOSCOPIC?

VANCE CYSTOSCOPIC is a medical device that received FDA 510(k) clearance on 1981-07-31. The listed applicant is Vance Products, Inc.. The 510(k) number is K812057.

When did VANCE CYSTOSCOPIC receive FDA 510(k) clearance?

VANCE CYSTOSCOPIC received FDA 510(k) clearance on 1981-07-31, under 510(k) number K812057.

Who is the listed applicant for VANCE CYSTOSCOPIC?

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 VANCE CYSTOSCOPIC?

The FDA product code for VANCE CYSTOSCOPIC is FBK.

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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.

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Related Devices (Code: FBK)

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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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