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FDA 510(k)

BERICHROM ALPHA-2-ANTIPLASMIN

K-Number: K884797 · 1989-04-21

ApplicantBehring Diagnostics, Inc.
Decision Date1989-04-21
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BERICHROM ALPHA-2-ANTIPLASMIN 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 1989-04-21 under 510(k) number K884797. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BERICHROM ALPHA-2-ANTIPLASMIN?

BERICHROM ALPHA-2-ANTIPLASMIN is a medical device that received FDA 510(k) clearance on 1989-04-21. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K884797.

When did BERICHROM ALPHA-2-ANTIPLASMIN receive FDA 510(k) clearance?

BERICHROM ALPHA-2-ANTIPLASMIN received FDA 510(k) clearance on 1989-04-21, under 510(k) number K884797.

Who is the listed applicant for BERICHROM ALPHA-2-ANTIPLASMIN?

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 BERICHROM ALPHA-2-ANTIPLASMIN?

The FDA product code for BERICHROM ALPHA-2-ANTIPLASMIN is GGP.

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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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