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FDA 510(k)

Cryocheck Chromogenic Factor VIII

K-Number: K193204 · 2020-07-17

Decision Date2020-07-17
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

Cryocheck Chromogenic Factor VIII is the device name listed in this FDA 510(k) record. The listed applicant is Precision Biologic. It received FDA 510(k) clearance on 2020-07-17 under 510(k) number K193204. 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 Cryocheck Chromogenic Factor VIII?

Cryocheck Chromogenic Factor VIII is a medical device that received FDA 510(k) clearance on 2020-07-17. The listed applicant is Precision Biologic. The 510(k) number is K193204.

When did Cryocheck Chromogenic Factor VIII receive FDA 510(k) clearance?

Cryocheck Chromogenic Factor VIII received FDA 510(k) clearance on 2020-07-17, under 510(k) number K193204.

Who is the listed applicant for Cryocheck Chromogenic Factor VIII?

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

What is the FDA product code for Cryocheck Chromogenic Factor VIII?

The FDA product code for Cryocheck Chromogenic Factor VIII is GGP.

Other records listing Precision Biologic as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: GGP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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