API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC
K-Number: K923684 · 1992-12-03
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Device Summary
Frequently Asked Questions
What is the API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC?
API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC is a medical device that received FDA 510(k) clearance on 1992-12-03. The listed applicant is Analytical Products, Inc.. The 510(k) number is K923684.
When did API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC receive FDA 510(k) clearance?
API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC received FDA 510(k) clearance on 1992-12-03, under 510(k) number K923684.
Who is the listed applicant for API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC?
The FDA 510(k) record lists Analytical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC?
The FDA product code for API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC is JWY.
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 Analytical 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.
Related Devices (Code: JWY)
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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