FDA 510(k)

SELECTIVE STREPTOCOCCUS AGAR

K-Number: K834005 · 1984-01-03

Decision Date1984-01-03

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SELECTIVE STREPTOCOCCUS AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K834005. 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 STREPTOCOCCUS AGAR?

SELECTIVE STREPTOCOCCUS AGAR is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Micro Media Laboratories. The 510(k) number is K834005.

When did SELECTIVE STREPTOCOCCUS AGAR receive FDA 510(k) clearance?

SELECTIVE STREPTOCOCCUS AGAR received FDA 510(k) clearance on 1984-01-03, under 510(k) number K834005.

Who is the listed applicant for SELECTIVE STREPTOCOCCUS AGAR?

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

What is the FDA product code for SELECTIVE STREPTOCOCCUS AGAR?

The FDA product code for SELECTIVE STREPTOCOCCUS AGAR is JSJ.

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Other records listing Micro Media Laboratories as applicant

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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.