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FDA 510(k)

SUSCEPTROL

K-Number: K820064 · 1982-01-28

ApplicantAmerican Type Culture Collection
Decision Date1982-01-28
Product CodeJTR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SUSCEPTROL is the device name listed in this FDA 510(k) record. The listed applicant is American Type Culture Collection. It received FDA 510(k) clearance on 1982-01-28 under 510(k) number K820064. The device is classified under product code JTR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUSCEPTROL?

SUSCEPTROL is a medical device that received FDA 510(k) clearance on 1982-01-28. The listed applicant is American Type Culture Collection. The 510(k) number is K820064.

When did SUSCEPTROL receive FDA 510(k) clearance?

SUSCEPTROL received FDA 510(k) clearance on 1982-01-28, under 510(k) number K820064.

Who is the listed applicant for SUSCEPTROL?

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

What is the FDA product code for SUSCEPTROL?

The FDA product code for SUSCEPTROL is JTR.

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Related Devices (Code: JTR)

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.

K871121PROTECT T.M.Pro-Lab, Inc.K862914FEKAL CHECK PARASITOLOGY CONTROL SLIDETrend Scientific, Inc.K861022KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMSMicro-Bio-LogicsK855198INDI KWIK (TM) CO/TWO KITMicro-Bio-LogicsK842579B.E.C. GROWTH CHEK MICROBIAL SUSPENSIONSBiological & Environmental Control LaboratoriesK842129LYFO-DISK MICROORGANISMSMicro-Bio-Logics

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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