FDA 510(k)

TRYPTIC SOY BROTH W/C02,CYSTEINE & 1%

K-Number: K800429 · 1980-03-19

Decision Date1980-03-19

Product CodeJSC

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

TRYPTIC SOY BROTH W/C02,CYSTEINE & 1% is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1980-03-19 under 510(k) number K800429. 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 W/C02,CYSTEINE & 1%?

TRYPTIC SOY BROTH W/C02,CYSTEINE & 1% is a medical device that received FDA 510(k) clearance on 1980-03-19. The listed applicant is Abbott Laboratories. The 510(k) number is K800429.

When did TRYPTIC SOY BROTH W/C02,CYSTEINE & 1% receive FDA 510(k) clearance?

TRYPTIC SOY BROTH W/C02,CYSTEINE & 1% received FDA 510(k) clearance on 1980-03-19, under 510(k) number K800429.

Who is the listed applicant for TRYPTIC SOY BROTH W/C02,CYSTEINE & 1%?

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

What is the FDA product code for TRYPTIC SOY BROTH W/C02,CYSTEINE & 1%?

The FDA product code for TRYPTIC SOY BROTH W/C02,CYSTEINE & 1% is JSC.

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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.