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FDA 510(k)

CIN AGAR MEDIUM

K-Number: K823050 · 1982-11-16

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1982-11-16
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CIN AGAR MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1982-11-16 under 510(k) number K823050. 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 CIN AGAR MEDIUM?

CIN AGAR MEDIUM is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K823050.

When did CIN AGAR MEDIUM receive FDA 510(k) clearance?

CIN AGAR MEDIUM received FDA 510(k) clearance on 1982-11-16, under 510(k) number K823050.

Who is the listed applicant for CIN AGAR MEDIUM?

The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIN AGAR MEDIUM?

The FDA product code for CIN AGAR MEDIUM is JSJ.

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Other records listing Gibco Laboratories Life Technologies, Inc. as applicant

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Related Devices (Code: JSJ)

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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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