CAPP TERMINAL DEVICE
K-Number: K780890 · 1978-06-13
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Device Summary
Frequently Asked Questions
What is the CAPP TERMINAL DEVICE?
CAPP TERMINAL DEVICE is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Hosmer Dorrance Corp.. The 510(k) number is K780890.
When did CAPP TERMINAL DEVICE receive FDA 510(k) clearance?
CAPP TERMINAL DEVICE received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780890.
Who is the listed applicant for CAPP TERMINAL DEVICE?
The FDA 510(k) record lists Hosmer Dorrance Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAPP TERMINAL DEVICE?
The FDA product code for CAPP TERMINAL DEVICE is IQX.
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 Hosmer Dorrance Corp. 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.
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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