STREP-ID PLATE
K-Number: K811422 · 1981-06-18
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Device Summary
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.
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
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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