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FDA 510(k)

MEKTOEN ENTERIC AGAR 100X15MM PLATE

K-Number: K791785 · 1979-10-01

Decision Date1979-10-01
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MEKTOEN ENTERIC AGAR 100X15MM PLATE is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Supply, Inc.. It received FDA 510(k) clearance on 1979-10-01 under 510(k) number K791785. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEKTOEN ENTERIC AGAR 100X15MM PLATE?

MEKTOEN ENTERIC AGAR 100X15MM PLATE is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K791785.

When did MEKTOEN ENTERIC AGAR 100X15MM PLATE receive FDA 510(k) clearance?

MEKTOEN ENTERIC AGAR 100X15MM PLATE received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791785.

Who is the listed applicant for MEKTOEN ENTERIC AGAR 100X15MM PLATE?

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

What is the FDA product code for MEKTOEN ENTERIC AGAR 100X15MM PLATE?

The FDA product code for MEKTOEN ENTERIC AGAR 100X15MM PLATE is JSI.

Related Clinical Trials

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.

Other records listing American Laboratory Supply, 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.

View all 36 devices →

Related Devices (Code: JSI)

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.

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.

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