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FDA 510(k)

UREA AGAR SLANT

K-Number: K811597 · 1981-06-25

ApplicantMicro Media Laboratories
Decision Date1981-06-25
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

UREA AGAR SLANT 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 1981-06-25 under 510(k) number K811597. 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 UREA AGAR SLANT?

UREA AGAR SLANT is a medical device that received FDA 510(k) clearance on 1981-06-25. The listed applicant is Micro Media Laboratories. The 510(k) number is K811597.

When did UREA AGAR SLANT receive FDA 510(k) clearance?

UREA AGAR SLANT received FDA 510(k) clearance on 1981-06-25, under 510(k) number K811597.

Who is the listed applicant for UREA AGAR SLANT?

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 UREA AGAR SLANT?

The FDA product code for UREA AGAR SLANT is JSH.

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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: JSH)

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.

K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia Manufacturers, 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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