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FDA 510(k)

AGAR, MOTILITY-NITRATE

K-Number: K790232 · 1979-02-21

ApplicantLos Angeles Biological Products
Decision Date1979-02-21
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AGAR, MOTILITY-NITRATE is the device name listed in this FDA 510(k) record. The listed applicant is Los Angeles Biological Products. It received FDA 510(k) clearance on 1979-02-21 under 510(k) number K790232. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGAR, MOTILITY-NITRATE?

AGAR, MOTILITY-NITRATE is a medical device that received FDA 510(k) clearance on 1979-02-21. The listed applicant is Los Angeles Biological Products. The 510(k) number is K790232.

When did AGAR, MOTILITY-NITRATE receive FDA 510(k) clearance?

AGAR, MOTILITY-NITRATE received FDA 510(k) clearance on 1979-02-21, under 510(k) number K790232.

Who is the listed applicant for AGAR, MOTILITY-NITRATE?

The FDA 510(k) record lists Los Angeles Biological Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AGAR, MOTILITY-NITRATE?

The FDA product code for AGAR, MOTILITY-NITRATE is JSE.

Related Clinical Trials

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Other records listing Los Angeles Biological Products 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.

K790229VAGINALIS, HAEMOPHILUSK790230DENTRIFICATION LACTOSE AGARK790231DECARBOXYLASE, BUFFERED LYSINE

Related Devices (Code: JSE)

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.

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy MediaK880116MRVP BROTHHardy MediaK874537KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGARLakewood Biochemical Co., Inc.

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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