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FDA 510(k)

FORGARTY CHIN PERIPHERAL INTRAOPERATIVE

K-Number: K830733 · 1983-04-18

ApplicantAmerican Edwards Laboratories
Decision Date1983-04-18
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FORGARTY CHIN PERIPHERAL INTRAOPERATIVE is the device name listed in this FDA 510(k) record. The listed applicant is American Edwards Laboratories. It received FDA 510(k) clearance on 1983-04-18 under 510(k) number K830733. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORGARTY CHIN PERIPHERAL INTRAOPERATIVE?

FORGARTY CHIN PERIPHERAL INTRAOPERATIVE is a medical device that received FDA 510(k) clearance on 1983-04-18. The listed applicant is American Edwards Laboratories. The 510(k) number is K830733.

When did FORGARTY CHIN PERIPHERAL INTRAOPERATIVE receive FDA 510(k) clearance?

FORGARTY CHIN PERIPHERAL INTRAOPERATIVE received FDA 510(k) clearance on 1983-04-18, under 510(k) number K830733.

Who is the listed applicant for FORGARTY CHIN PERIPHERAL INTRAOPERATIVE?

The FDA 510(k) record lists American Edwards Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORGARTY CHIN PERIPHERAL INTRAOPERATIVE?

The FDA product code for FORGARTY CHIN PERIPHERAL INTRAOPERATIVE is LIT.

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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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