VIRAPURE, CHLAMYPURE AND MYCOPURE
K-Number: K914894 · 1991-12-18
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Device Summary
Frequently Asked Questions
What is the VIRAPURE, CHLAMYPURE AND MYCOPURE?
VIRAPURE, CHLAMYPURE AND MYCOPURE is a medical device that received FDA 510(k) clearance on 1991-12-18. The listed applicant is Microtest. The 510(k) number is K914894.
When did VIRAPURE, CHLAMYPURE AND MYCOPURE receive FDA 510(k) clearance?
VIRAPURE, CHLAMYPURE AND MYCOPURE received FDA 510(k) clearance on 1991-12-18, under 510(k) number K914894.
Who is the listed applicant for VIRAPURE, CHLAMYPURE AND MYCOPURE?
The FDA 510(k) record lists Microtest as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIRAPURE, CHLAMYPURE AND MYCOPURE?
The FDA product code for VIRAPURE, CHLAMYPURE AND MYCOPURE is JSM.
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 Microtest 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: JSM)
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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