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FDA 510(k)

REAGENTS

K-Number: K840030 · 1984-03-02

ApplicantAnaerobe Systems
Decision Date1984-03-02
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

REAGENTS is the device name listed in this FDA 510(k) record. The listed applicant is Anaerobe Systems. It received FDA 510(k) clearance on 1984-03-02 under 510(k) number K840030. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENTS?

REAGENTS is a medical device that received FDA 510(k) clearance on 1984-03-02. The listed applicant is Anaerobe Systems. The 510(k) number is K840030.

When did REAGENTS receive FDA 510(k) clearance?

REAGENTS received FDA 510(k) clearance on 1984-03-02, under 510(k) number K840030.

Who is the listed applicant for REAGENTS?

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

What is the FDA product code for REAGENTS?

The FDA product code for REAGENTS is JTO.

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Related Devices (Code: JTO)

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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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