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FDA 510(k)

CLED AGAR WITH ANDRADES INDICATOR

K-Number: K864239 · 1987-03-31

ApplicantMds Laboratories, Inc.
Decision Date1987-03-31
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CLED AGAR WITH ANDRADES INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mds Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K864239. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLED AGAR WITH ANDRADES INDICATOR?

CLED AGAR WITH ANDRADES INDICATOR is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864239.

When did CLED AGAR WITH ANDRADES INDICATOR receive FDA 510(k) clearance?

CLED AGAR WITH ANDRADES INDICATOR received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864239.

Who is the listed applicant for CLED AGAR WITH ANDRADES INDICATOR?

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

What is the FDA product code for CLED AGAR WITH ANDRADES INDICATOR?

The FDA product code for CLED AGAR WITH ANDRADES INDICATOR is JSH.

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Other records listing Mds Laboratories, 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.

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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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