MICROTIME
K-Number: K952616 · 1995-09-27
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Device Summary
Frequently Asked Questions
What is the MICROTIME?
MICROTIME is a medical device that received FDA 510(k) clearance on 1995-09-27. The listed applicant is Westmed Intl.. The 510(k) number is K952616.
When did MICROTIME receive FDA 510(k) clearance?
MICROTIME received FDA 510(k) clearance on 1995-09-27, under 510(k) number K952616.
Who is the listed applicant for MICROTIME?
The FDA 510(k) record lists Westmed Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROTIME?
The FDA product code for MICROTIME is BTI.
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 Westmed Intl. 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: BTI)
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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