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FDA 510(k)

FREEZE DRIED FICIN

K-Number: K813404 · 1982-02-10

ApplicantBiological Corp. of America
Decision Date1982-02-10
Product CodeKSK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FREEZE DRIED FICIN is the device name listed in this FDA 510(k) record. The listed applicant is Biological Corp. of America. It received FDA 510(k) clearance on 1982-02-10 under 510(k) number K813404. The device is classified under product code KSK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEZE DRIED FICIN?

FREEZE DRIED FICIN is a medical device that received FDA 510(k) clearance on 1982-02-10. The listed applicant is Biological Corp. of America. The 510(k) number is K813404.

When did FREEZE DRIED FICIN receive FDA 510(k) clearance?

FREEZE DRIED FICIN received FDA 510(k) clearance on 1982-02-10, under 510(k) number K813404.

Who is the listed applicant for FREEZE DRIED FICIN?

The FDA 510(k) record lists Biological Corp. of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREEZE DRIED FICIN?

The FDA product code for FREEZE DRIED FICIN is KSK.

Related Clinical Trials

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.

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Other records listing Biological Corp. of America 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.

K812565ELUTION SOLUTIONK812222EM-XK810803FREEZE DRIED PAPAINK781397EM-VK760162HEMATOLOGY CONTROL

Related Devices (Code: KSK)

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.

K813342GAMMA CHLOROQUINE DIPHOSPHATE SOLUTIONGamma Biologicals, Inc.K810803FREEZE DRIED PAPAINBiological Corp. of AmericaK780962AUTOMATED ENZYMEHyland Therapeutic Div., Travenol LaboratoriesK760123AUTOZYMEBd Becton Dickinson Vacutainer Systems Preanalytic

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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