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FDA 510(k)

LAURYL TRYPTOSE BROTH

K-Number: K791481 · 1979-08-22

Decision Date1979-08-22
Product CodeJSD
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LAURYL TRYPTOSE BROTH is the device name listed in this FDA 510(k) record. The listed applicant is Isle Media and Sterile Products, Inc.. It received FDA 510(k) clearance on 1979-08-22 under 510(k) number K791481. The device is classified under product code JSD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAURYL TRYPTOSE BROTH?

LAURYL TRYPTOSE BROTH is a medical device that received FDA 510(k) clearance on 1979-08-22. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K791481.

When did LAURYL TRYPTOSE BROTH receive FDA 510(k) clearance?

LAURYL TRYPTOSE BROTH received FDA 510(k) clearance on 1979-08-22, under 510(k) number K791481.

Who is the listed applicant for LAURYL TRYPTOSE BROTH?

The FDA 510(k) record lists Isle Media and Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAURYL TRYPTOSE BROTH?

The FDA product code for LAURYL TRYPTOSE BROTH is JSD.

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 Isle Media and Sterile Products, Inc. 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 93 devices →

Related Devices (Code: JSD)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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