STREP ID QUAD
K-Number: K832863 · 1983-09-26
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Device Summary
Frequently Asked Questions
What is the STREP ID QUAD?
STREP ID QUAD is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Troy Biologicals, Inc.. The 510(k) number is K832863.
When did STREP ID QUAD receive FDA 510(k) clearance?
STREP ID QUAD received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832863.
Who is the listed applicant for STREP ID QUAD?
The FDA 510(k) record lists Troy Biologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STREP ID QUAD?
The FDA product code for STREP ID QUAD 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 Troy Biologicals, 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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