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FDA 510(k)

#2008 SIMMONS CITRATE

K-Number: K820809 · 1982-04-08

ApplicantBiomedica, Inc.
Decision Date1982-04-08
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

#2008 SIMMONS CITRATE is the device name listed in this FDA 510(k) record. The listed applicant is Biomedica, Inc.. It received FDA 510(k) clearance on 1982-04-08 under 510(k) number K820809. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the #2008 SIMMONS CITRATE?

#2008 SIMMONS CITRATE is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is Biomedica, Inc.. The 510(k) number is K820809.

When did #2008 SIMMONS CITRATE receive FDA 510(k) clearance?

#2008 SIMMONS CITRATE received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820809.

Who is the listed applicant for #2008 SIMMONS CITRATE?

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

What is the FDA product code for #2008 SIMMONS CITRATE?

The FDA product code for #2008 SIMMONS CITRATE is JSF.

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Other records listing Biomedica, Inc. 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.

K820793#1904L MUELLER HINTON W/5% SHEEP BLOODK820803#2003 MYCOBIOTIC AGARK820802#2009 BIGGY AGARK820800#2006 SALMONELLA SHIGELLA AGARK820791#4005 TSA SLANT-TUBED MEDIAK820794#19012 CHOCOLATE MUELLER HINTON-150X15MM

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Related Devices (Code: JSF)

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.

K880946NUTRIENT GELATIN - PRODUCT NUMBER T2860Lakewood Biochemical Co., Inc.K880126LAURYL TRYPTOSE BROTHHardy MediaK880119MOELLERS DECARBOXYLASE, ONITHINEHardy MediaK880120MOELLERS DECARBOXYLASE, LYSINEHardy MediaK880139ONPG TEST REAGENTHardy MediaK880113CYSTINE TRYPTIC MEDIUM W/LACTOSEHardy Media

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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