FDA 510(k)

SALTIME VISCOMETER

K-Number: K936006 · 1996-02-09

Decision Date1996-02-09

Product CodeLHZ

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

SALTIME VISCOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Harold J. Kosasky, M.D.. It received FDA 510(k) clearance on 1996-02-09 under 510(k) number K936006. The device is classified under product code LHZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALTIME VISCOMETER?

SALTIME VISCOMETER is a medical device that received FDA 510(k) clearance on 1996-02-09. The listed applicant is Harold J. Kosasky, M.D.. The 510(k) number is K936006.

When did SALTIME VISCOMETER receive FDA 510(k) clearance?

SALTIME VISCOMETER received FDA 510(k) clearance on 1996-02-09, under 510(k) number K936006.

Who is the listed applicant for SALTIME VISCOMETER?

The FDA 510(k) record lists Harold J. Kosasky, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SALTIME VISCOMETER?

The FDA product code for SALTIME VISCOMETER is LHZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.