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FDA 510(k)

BEHRING COAGULATION TIMER

K-Number: K955278 · 1996-05-30

ApplicantBehring Diagnostics, Inc.
Decision Date1996-05-30
Product CodeGGN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BEHRING COAGULATION TIMER is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1996-05-30 under 510(k) number K955278. The device is classified under product code GGN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEHRING COAGULATION TIMER?

BEHRING COAGULATION TIMER is a medical device that received FDA 510(k) clearance on 1996-05-30. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K955278.

When did BEHRING COAGULATION TIMER receive FDA 510(k) clearance?

BEHRING COAGULATION TIMER received FDA 510(k) clearance on 1996-05-30, under 510(k) number K955278.

Who is the listed applicant for BEHRING COAGULATION TIMER?

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

What is the FDA product code for BEHRING COAGULATION TIMER?

The FDA product code for BEHRING COAGULATION TIMER is GGN.

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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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