FDA 510(k)

BIOVATION URINALYSIS REPORTER

K-Number: K812604 · 1981-10-02

Decision Date1981-10-02

Product CodeJQP

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

BIOVATION URINALYSIS REPORTER is the device name listed in this FDA 510(k) record. The listed applicant is Biovation, Inc.. It received FDA 510(k) clearance on 1981-10-02 under 510(k) number K812604. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOVATION URINALYSIS REPORTER?

BIOVATION URINALYSIS REPORTER is a medical device that received FDA 510(k) clearance on 1981-10-02. The listed applicant is Biovation, Inc.. The 510(k) number is K812604.

When did BIOVATION URINALYSIS REPORTER receive FDA 510(k) clearance?

BIOVATION URINALYSIS REPORTER received FDA 510(k) clearance on 1981-10-02, under 510(k) number K812604.

Who is the listed applicant for BIOVATION URINALYSIS REPORTER?

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

What is the FDA product code for BIOVATION URINALYSIS REPORTER?

The FDA product code for BIOVATION URINALYSIS REPORTER is JQP.

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Other records listing Biovation, Inc. as applicant

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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.