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FDA 510(k)

STREP-ID PLATE

K-Number: K811422 · 1981-06-18

Decision Date1981-06-18
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

STREP-ID PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. It received FDA 510(k) clearance on 1981-06-18 under 510(k) number K811422. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STREP-ID PLATE?

STREP-ID PLATE is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K811422.

When did STREP-ID PLATE receive FDA 510(k) clearance?

STREP-ID PLATE received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811422.

Who is the listed applicant for STREP-ID PLATE?

The FDA 510(k) record lists Carr-Scarborough Microbiologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STREP-ID PLATE?

The FDA product code for STREP-ID PLATE is JSI.

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 Carr-Scarborough Microbiologicals, 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 24 devices →

Related Devices (Code: JSI)

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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