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FDA 510(k)

TRYPTIC SOY BROTH MEDIA

K-Number: K832620 · 1983-09-12

Decision Date1983-09-12
Product CodeJSC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRYPTIC SOY BROTH MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Carroll Biological Corp.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832620. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPTIC SOY BROTH MEDIA?

TRYPTIC SOY BROTH MEDIA is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Carroll Biological Corp.. The 510(k) number is K832620.

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

TRYPTIC SOY BROTH MEDIA received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832620.

Who is the listed applicant for TRYPTIC SOY BROTH MEDIA?

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

What is the FDA product code for TRYPTIC SOY BROTH MEDIA?

The FDA product code for TRYPTIC SOY BROTH MEDIA is JSC.

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 Carroll Biological Corp. 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 11 devices →

Related Devices (Code: JSC)

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.

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