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FDA 510(k)

NEEDLES USED IN ANGIOGRAPHIC PROCED.

K-Number: K772369 · 1978-01-24

ApplicantArgon Medical Corp.
Decision Date1978-01-24
Product CodeDRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NEEDLES USED IN ANGIOGRAPHIC PROCED. is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1978-01-24 under 510(k) number K772369. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLES USED IN ANGIOGRAPHIC PROCED.?

NEEDLES USED IN ANGIOGRAPHIC PROCED. is a medical device that received FDA 510(k) clearance on 1978-01-24. The listed applicant is Argon Medical Corp.. The 510(k) number is K772369.

When did NEEDLES USED IN ANGIOGRAPHIC PROCED. receive FDA 510(k) clearance?

NEEDLES USED IN ANGIOGRAPHIC PROCED. received FDA 510(k) clearance on 1978-01-24, under 510(k) number K772369.

Who is the listed applicant for NEEDLES USED IN ANGIOGRAPHIC PROCED.?

The FDA 510(k) record lists Argon Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLES USED IN ANGIOGRAPHIC PROCED.?

The FDA product code for NEEDLES USED IN ANGIOGRAPHIC PROCED. is DRC.

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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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