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FDA 510(k)

SELECTIVE CULTURE MED. SELECTIVE STREP

K-Number: K841839 · 1984-05-25

ApplicantMicroline Scientific
Decision Date1984-05-25
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SELECTIVE CULTURE MED. SELECTIVE STREP is the device name listed in this FDA 510(k) record. The listed applicant is Microline Scientific. It received FDA 510(k) clearance on 1984-05-25 under 510(k) number K841839. 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 SELECTIVE CULTURE MED. SELECTIVE STREP?

SELECTIVE CULTURE MED. SELECTIVE STREP is a medical device that received FDA 510(k) clearance on 1984-05-25. The listed applicant is Microline Scientific. The 510(k) number is K841839.

When did SELECTIVE CULTURE MED. SELECTIVE STREP receive FDA 510(k) clearance?

SELECTIVE CULTURE MED. SELECTIVE STREP received FDA 510(k) clearance on 1984-05-25, under 510(k) number K841839.

Who is the listed applicant for SELECTIVE CULTURE MED. SELECTIVE STREP?

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

What is the FDA product code for SELECTIVE CULTURE MED. SELECTIVE STREP?

The FDA product code for SELECTIVE CULTURE MED. SELECTIVE STREP is JSJ.

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Other records listing Microline Scientific 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.

K841845SELECTIVE CULTURE MED. COLUMBIA CNAK841586CHOCOLATE AGARK841844DIFFERENTIAL CULTURE MEDIUM-BIGGY AGARK841842DIFFERENTIAL CULTURE MED. MACCONKEY AGARK841843DIFFERENTIAL CULTURE MED. LEVINE EMBK841840SELECTIVE CULTURE MED. PHENYLETHYL ALCO

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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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