WEIL PERFUSOMETER #100
K-Number: K830429 · 1983-10-31
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Device Summary
Frequently Asked Questions
What is the WEIL PERFUSOMETER #100?
WEIL PERFUSOMETER #100 is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Wescor, Inc.. The 510(k) number is K830429.
When did WEIL PERFUSOMETER #100 receive FDA 510(k) clearance?
WEIL PERFUSOMETER #100 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K830429.
Who is the listed applicant for WEIL PERFUSOMETER #100?
The FDA 510(k) record lists Wescor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WEIL PERFUSOMETER #100?
The FDA product code for WEIL PERFUSOMETER #100 is FLL.
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 Wescor, 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: FLL)
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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