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FDA 510(k)

STACHROM ANTIPLASMIN CONTROL

K-Number: K882603 · 1988-09-02

ApplicantAmerican Bioproducts Co.
Decision Date1988-09-02
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

STACHROM ANTIPLASMIN CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is American Bioproducts Co.. It received FDA 510(k) clearance on 1988-09-02 under 510(k) number K882603. 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 STACHROM ANTIPLASMIN CONTROL?

STACHROM ANTIPLASMIN CONTROL is a medical device that received FDA 510(k) clearance on 1988-09-02. The listed applicant is American Bioproducts Co.. The 510(k) number is K882603.

When did STACHROM ANTIPLASMIN CONTROL receive FDA 510(k) clearance?

STACHROM ANTIPLASMIN CONTROL received FDA 510(k) clearance on 1988-09-02, under 510(k) number K882603.

Who is the listed applicant for STACHROM ANTIPLASMIN CONTROL?

The FDA 510(k) record lists American Bioproducts Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STACHROM ANTIPLASMIN CONTROL?

The FDA product code for STACHROM ANTIPLASMIN CONTROL is GGP.

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Other records listing American Bioproducts Co. 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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