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FDA 510(k)

MOTILITY INDOLE ORNITHINE-MEDIUM

K-Number: K834003 · 1983-12-22

ApplicantMicro Media Laboratories
Decision Date1983-12-22
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MOTILITY INDOLE ORNITHINE-MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1983-12-22 under 510(k) number K834003. 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 MOTILITY INDOLE ORNITHINE-MEDIUM?

MOTILITY INDOLE ORNITHINE-MEDIUM is a medical device that received FDA 510(k) clearance on 1983-12-22. The listed applicant is Micro Media Laboratories. The 510(k) number is K834003.

When did MOTILITY INDOLE ORNITHINE-MEDIUM receive FDA 510(k) clearance?

MOTILITY INDOLE ORNITHINE-MEDIUM received FDA 510(k) clearance on 1983-12-22, under 510(k) number K834003.

Who is the listed applicant for MOTILITY INDOLE ORNITHINE-MEDIUM?

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

What is the FDA product code for MOTILITY INDOLE ORNITHINE-MEDIUM?

The FDA product code for MOTILITY INDOLE ORNITHINE-MEDIUM is JSE.

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Other records listing Micro Media Laboratories 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.

K853690COLUMBIZ BLOOD AGARK853691TERGITOL 7 AGARK851344OXIDATIVE FORMENTIVE MEDIUMK851345PURPLE BROTHK851343BROM CRESOL PURPLE STARCHK851348COBA AGAR

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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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