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FDA 510(k)

CYSTINE TRYPTIC MEDIUM

K-Number: K834007 · 1983-12-22

ApplicantMicro Media Laboratories
Decision Date1983-12-22
Product CodeJSQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CYSTINE TRYPTIC MEDIUM 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 1983-12-22 under 510(k) number K834007. The device is classified under product code JSQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYSTINE TRYPTIC MEDIUM?

CYSTINE TRYPTIC MEDIUM is a medical device that received FDA 510(k) clearance on 1983-12-22. The listed applicant is Micro Media Laboratories. The 510(k) number is K834007.

When did CYSTINE TRYPTIC MEDIUM receive FDA 510(k) clearance?

CYSTINE TRYPTIC MEDIUM received FDA 510(k) clearance on 1983-12-22, under 510(k) number K834007.

Who is the listed applicant for CYSTINE TRYPTIC MEDIUM?

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 CYSTINE TRYPTIC MEDIUM?

The FDA product code for CYSTINE TRYPTIC MEDIUM is JSQ.

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Other records listing Micro Media Laboratories 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.

K853690COLUMBIZ BLOOD AGARK853691TERGITOL 7 AGARK851344OXIDATIVE FORMENTIVE MEDIUMK851345PURPLE BROTHK851343BROM CRESOL PURPLE STARCHK851348COBA AGAR

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Related Devices (Code: JSQ)

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.

K811138NUTRIENT AGARAcumedia Manufacturers, Inc.K761226GP3%SP-2100DOHON100/120 MESH SUPELCOPORTSupelco, 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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