FLOWMETER, P.C., REDESIGNED VERSION
K-Number: K760102 · 1976-07-16
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Device Summary
Frequently Asked Questions
What is the FLOWMETER, P.C., REDESIGNED VERSION?
FLOWMETER, P.C., REDESIGNED VERSION is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Ohio Medical Products. The 510(k) number is K760102.
When did FLOWMETER, P.C., REDESIGNED VERSION receive FDA 510(k) clearance?
FLOWMETER, P.C., REDESIGNED VERSION received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760102.
Who is the listed applicant for FLOWMETER, P.C., REDESIGNED VERSION?
The FDA 510(k) record lists Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOWMETER, P.C., REDESIGNED VERSION?
The FDA product code for FLOWMETER, P.C., REDESIGNED VERSION is CAX.
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 Ohio Medical Products 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: CAX)
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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