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FDA 510(k)

BEHRING TURBITIMER

K-Number: K883646 · 1988-10-31

ApplicantBehring Diagnostics, Inc.
Decision Date1988-10-31
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BEHRING TURBITIMER 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 1988-10-31 under 510(k) number K883646. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEHRING TURBITIMER?

BEHRING TURBITIMER is a medical device that received FDA 510(k) clearance on 1988-10-31. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K883646.

When did BEHRING TURBITIMER receive FDA 510(k) clearance?

BEHRING TURBITIMER received FDA 510(k) clearance on 1988-10-31, under 510(k) number K883646.

Who is the listed applicant for BEHRING TURBITIMER?

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 TURBITIMER?

The FDA product code for BEHRING TURBITIMER is JJQ.

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Other records listing Behring Diagnostics, Inc. as applicant

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Related Devices (Code: JJQ)

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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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