FDA 510(k)

AGAR P

K-Number: K823102 · 1982-12-03

Decision Date1982-12-03

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

AGAR P is the device name listed in this FDA 510(k) record. The listed applicant is Dms Laboratories. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823102. 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 AGAR P?

AGAR P is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Dms Laboratories. The 510(k) number is K823102.

When did AGAR P receive FDA 510(k) clearance?

AGAR P received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823102.

Who is the listed applicant for AGAR P?

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

What is the FDA product code for AGAR P?

The FDA product code for AGAR P is JSJ.

Other records listing Dms 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.

K831186RAPID NFT K831187TRP K830437CHS K821038FAST VIOLET B K813613RAPID CH K813612RAPID ZYME

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Related Devices (Code: JSJ)

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.