Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TRYPTIC SOY AGAR

K-Number: K811612 · 1981-06-25

Decision Date1981-06-25
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRYPTIC SOY 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 1981-06-25 under 510(k) number K811612. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPTIC SOY AGAR?

TRYPTIC SOY AGAR is a medical device that received FDA 510(k) clearance on 1981-06-25. The listed applicant is Micro Media Laboratories. The 510(k) number is K811612.

When did TRYPTIC SOY AGAR receive FDA 510(k) clearance?

TRYPTIC SOY AGAR received FDA 510(k) clearance on 1981-06-25, under 510(k) number K811612.

Who is the listed applicant for TRYPTIC SOY 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 TRYPTIC SOY AGAR?

The FDA product code for TRYPTIC SOY AGAR is JSG.

Related Clinical Trials

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.

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.

View all 52 devices →

Related Devices (Code: JSG)

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.

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.

↑