FDA 510(k)

TERGITOL 7 BROTH

K-Number: K881561 · 1988-04-18

Decision Date1988-04-18

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

TERGITOL 7 BROTH 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 1988-04-18 under 510(k) number K881561. 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 TERGITOL 7 BROTH?

TERGITOL 7 BROTH is a medical device that received FDA 510(k) clearance on 1988-04-18. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K881561.

When did TERGITOL 7 BROTH receive FDA 510(k) clearance?

TERGITOL 7 BROTH received FDA 510(k) clearance on 1988-04-18, under 510(k) number K881561.

Who is the listed applicant for TERGITOL 7 BROTH?

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 TERGITOL 7 BROTH?

The FDA product code for TERGITOL 7 BROTH is JSJ.

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Other records listing Acumedia Manufacturers, Inc. as applicant

K881540FLO AGAR K881569STUARTS TRANSPORT MEDIUM K881544LITTMAN AGAR K881575SELECTIVE STREPTOCOCCUS AGAR K881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGAR K881567WILKENS CHALGREN AGAR

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Related Devices (Code: JSJ)

K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421Lakewood Biochemical Co., Inc.K881544LITTMAN AGARAcumedia Manufacturers, Inc.K881526CHAPMAN STONE MEDIUMAcumedia Manufacturers, Inc.K881571YM BROTHAcumedia Manufacturers, Inc.K881578STREPTOSELAcumedia Manufacturers, Inc.K881549MYCOLOGICAL AGAR W/LOW PHAcumedia 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.