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FDA 510(k)

MOTILITY TEST MEDIUM

K-Number: K833216 · 1983-10-27

ApplicantAcumedia Manufacturers, Inc.
Decision Date1983-10-27
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MOTILITY TEST MEDIUM 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 1983-10-27 under 510(k) number K833216. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTILITY TEST MEDIUM?

MOTILITY TEST MEDIUM is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833216.

When did MOTILITY TEST MEDIUM receive FDA 510(k) clearance?

MOTILITY TEST MEDIUM received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833216.

Who is the listed applicant for MOTILITY TEST MEDIUM?

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 MOTILITY TEST MEDIUM?

The FDA product code for MOTILITY TEST MEDIUM is JSH.

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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

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Related Devices (Code: JSH)

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.

K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia 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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