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FDA 510(k)

MODIFICATION OF BEHRING RAPIMAT II/T

K-Number: K882095 · 1988-08-02

ApplicantBehring Diagnostics, Inc.
Decision Date1988-08-02
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF BEHRING RAPIMAT II/T 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 1988-08-02 under 510(k) number K882095. 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 MODIFICATION OF BEHRING RAPIMAT II/T?

MODIFICATION OF BEHRING RAPIMAT II/T is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K882095.

When did MODIFICATION OF BEHRING RAPIMAT II/T receive FDA 510(k) clearance?

MODIFICATION OF BEHRING RAPIMAT II/T received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882095.

Who is the listed applicant for MODIFICATION OF BEHRING RAPIMAT II/T?

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 MODIFICATION OF BEHRING RAPIMAT II/T?

The FDA product code for MODIFICATION OF BEHRING RAPIMAT II/T is JJQ.

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Other records listing Behring Diagnostics, 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.

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