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FDA 510(k)

TRAP-BLOOD VESSEL STABILIZATION DEVICE

K-Number: K781072 · 1978-08-10

ApplicantAyer, Patrick, M.D.
Decision Date1978-08-10
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TRAP-BLOOD VESSEL STABILIZATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Ayer, Patrick, M.D.. It received FDA 510(k) clearance on 1978-08-10 under 510(k) number K781072. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAP-BLOOD VESSEL STABILIZATION DEVICE?

TRAP-BLOOD VESSEL STABILIZATION DEVICE is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Ayer, Patrick, M.D.. The 510(k) number is K781072.

When did TRAP-BLOOD VESSEL STABILIZATION DEVICE receive FDA 510(k) clearance?

TRAP-BLOOD VESSEL STABILIZATION DEVICE received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781072.

Who is the listed applicant for TRAP-BLOOD VESSEL STABILIZATION DEVICE?

The FDA 510(k) record lists Ayer, Patrick, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRAP-BLOOD VESSEL STABILIZATION DEVICE?

The FDA product code for TRAP-BLOOD VESSEL STABILIZATION DEVICE is JIT.

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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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