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FDA 510(k)

PATHROMTIN

K-Number: K932011 · 1993-10-25

ApplicantBehring Diagnostics, Inc.
Decision Date1993-10-25
Product CodeGFO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PATHROMTIN 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 1993-10-25 under 510(k) number K932011. The device is classified under product code GFO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATHROMTIN?

PATHROMTIN is a medical device that received FDA 510(k) clearance on 1993-10-25. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K932011.

When did PATHROMTIN receive FDA 510(k) clearance?

PATHROMTIN received FDA 510(k) clearance on 1993-10-25, under 510(k) number K932011.

Who is the listed applicant for PATHROMTIN?

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 PATHROMTIN?

The FDA product code for PATHROMTIN is GFO.

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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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