FDA 510(k)

REAGENTS FOR SERODIAGNOSIS OF ASPERGILL

K-Number: K812740 · 1981-10-20

ApplicantNolan Biological Laboratories, Inc.

Decision Date1981-10-20

Product CodeJWT

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

REAGENTS FOR SERODIAGNOSIS OF ASPERGILL is the device name listed in this FDA 510(k) record. The listed applicant is Nolan Biological Laboratories, Inc.. It received FDA 510(k) clearance on 1981-10-20 under 510(k) number K812740. The device is classified under product code JWT. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENTS FOR SERODIAGNOSIS OF ASPERGILL?

REAGENTS FOR SERODIAGNOSIS OF ASPERGILL is a medical device that received FDA 510(k) clearance on 1981-10-20. The listed applicant is Nolan Biological Laboratories, Inc.. The 510(k) number is K812740.

When did REAGENTS FOR SERODIAGNOSIS OF ASPERGILL receive FDA 510(k) clearance?

REAGENTS FOR SERODIAGNOSIS OF ASPERGILL received FDA 510(k) clearance on 1981-10-20, under 510(k) number K812740.

Who is the listed applicant for REAGENTS FOR SERODIAGNOSIS OF ASPERGILL?

The FDA 510(k) record lists Nolan Biological Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REAGENTS FOR SERODIAGNOSIS OF ASPERGILL?

The FDA product code for REAGENTS FOR SERODIAGNOSIS OF ASPERGILL is JWT.

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Other records listing Nolan Biological Laboratories, Inc. as applicant

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Related Devices (Code: JWT)

K792700ASPERGILLUS SP, COMPLEMENT FIXATIONMeridian Diagnostics, Inc.K791387ASPERGILLUS MYCELIAL ANTIGEN #CF10024XImmuno-Mycologics, Inc.K790672ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVUDiagnostica, Inc.K760830ASPERGILLUS MYCELIAL ANTIGENI M, Inc.

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.