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FDA 510(k)

BLOOD AGAR W/AMPICILLIN

K-Number: K840554 · 1984-02-27

ApplicantRemel Co.
Decision Date1984-02-27
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BLOOD AGAR W/AMPICILLIN is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1984-02-27 under 510(k) number K840554. 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 BLOOD AGAR W/AMPICILLIN?

BLOOD AGAR W/AMPICILLIN is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Remel Co.. The 510(k) number is K840554.

When did BLOOD AGAR W/AMPICILLIN receive FDA 510(k) clearance?

BLOOD AGAR W/AMPICILLIN received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840554.

Who is the listed applicant for BLOOD AGAR W/AMPICILLIN?

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

What is the FDA product code for BLOOD AGAR W/AMPICILLIN?

The FDA product code for BLOOD AGAR W/AMPICILLIN is JSJ.

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Other records listing Remel Co. 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.

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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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