MICROVAC
K-Number: K801134 · 1980-05-30
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Device Summary
Frequently Asked Questions
What is the MICROVAC?
MICROVAC is a medical device that received FDA 510(k) clearance on 1980-05-30. The listed applicant is Progress Mankind Technology. The 510(k) number is K801134.
When did MICROVAC receive FDA 510(k) clearance?
MICROVAC received FDA 510(k) clearance on 1980-05-30, under 510(k) number K801134.
Who is the listed applicant for MICROVAC?
The FDA 510(k) record lists Progress Mankind Technology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROVAC?
The FDA product code for MICROVAC is JOL.
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 Progress Mankind Technology 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: JOL)
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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