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FDA 510(k)

CAMPY BLOOD AGAR

K-Number: K792674 · 1980-01-28

ApplicantRegional Media Laboratories
Decision Date1980-01-28
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CAMPY BLOOD AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Regional Media Laboratories. It received FDA 510(k) clearance on 1980-01-28 under 510(k) number K792674. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPY BLOOD AGAR?

CAMPY BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Regional Media Laboratories. The 510(k) number is K792674.

When did CAMPY BLOOD AGAR receive FDA 510(k) clearance?

CAMPY BLOOD AGAR received FDA 510(k) clearance on 1980-01-28, under 510(k) number K792674.

Who is the listed applicant for CAMPY BLOOD AGAR?

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

What is the FDA product code for CAMPY BLOOD AGAR?

The FDA product code for CAMPY BLOOD AGAR is JSJ.

Related Clinical Trials

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Other records listing Regional 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.

K894848HAEMOPHILUS TEST MEDIUM (BROTH)

Related Devices (Code: JSJ)

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.

K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421Lakewood Biochemical Co., Inc.K881544LITTMAN AGARAcumedia Manufacturers, Inc.K881561TERGITOL 7 BROTHAcumedia Manufacturers, Inc.K881526CHAPMAN STONE MEDIUMAcumedia Manufacturers, Inc.K881571YM BROTHAcumedia Manufacturers, Inc.K881578STREPTOSELAcumedia 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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