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FDA 510(k)

CAPP TERMINAL DEVICE

K-Number: K780890 · 1978-06-13

Decision Date1978-06-13
Product CodeIQX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CAPP TERMINAL DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Hosmer Dorrance Corp.. It received FDA 510(k) clearance on 1978-06-13 under 510(k) number K780890. The device is classified under product code IQX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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