FDA 510(k)

SCHAEDLER BROTH

K-Number: K811329 · 1981-05-29

Decision Date1981-05-29

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SCHAEDLER 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 1981-05-29 under 510(k) number K811329. 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 SCHAEDLER BROTH?

SCHAEDLER BROTH is a medical device that received FDA 510(k) clearance on 1981-05-29. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811329.

When did SCHAEDLER BROTH receive FDA 510(k) clearance?

SCHAEDLER BROTH received FDA 510(k) clearance on 1981-05-29, under 510(k) number K811329.

Who is the listed applicant for SCHAEDLER 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 SCHAEDLER BROTH?

The FDA product code for SCHAEDLER BROTH is JSJ.

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Other records listing Acumedia Manufacturers, Inc. as applicant

K881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGAR K881540FLO AGAR K881544LITTMAN AGAR K881561TERGITOL 7 BROTH K881575SELECTIVE STREPTOCOCCUS AGAR K881569STUARTS TRANSPORT MEDIUM

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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.