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FDA 510(k)

DCLS AGAR

K-Number: K811736 · 1981-07-02

ApplicantAcumedia Manufacturers, Inc.
Decision Date1981-07-02
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DCLS AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Acumedia Manufacturers, Inc.. It received FDA 510(k) clearance on 1981-07-02 under 510(k) number K811736. 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 DCLS AGAR?

DCLS AGAR is a medical device that received FDA 510(k) clearance on 1981-07-02. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811736.

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

DCLS AGAR received FDA 510(k) clearance on 1981-07-02, under 510(k) number K811736.

Who is the listed applicant for DCLS AGAR?

The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DCLS AGAR?

The FDA product code for DCLS AGAR is JSJ.

Other records listing Acumedia Manufacturers, Inc. 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.

K881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGARK881540FLO AGARK881544LITTMAN AGARK881561TERGITOL 7 BROTHK881575SELECTIVE STREPTOCOCCUS AGARK881569STUARTS TRANSPORT MEDIUM

View all 177 devices →

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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