FDA 510(k)

SITE COAXIAL I/A HANDPIECE 30 TIP

K-Number: K840965 · 1984-05-09

Decision Date1984-05-09

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

SITE COAXIAL I/A HANDPIECE 30 TIP is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K840965. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SITE COAXIAL I/A HANDPIECE 30 TIP?

SITE COAXIAL I/A HANDPIECE 30 TIP is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Chiron Vision Corp.. The 510(k) number is K840965.

When did SITE COAXIAL I/A HANDPIECE 30 TIP receive FDA 510(k) clearance?

SITE COAXIAL I/A HANDPIECE 30 TIP received FDA 510(k) clearance on 1984-05-09, under 510(k) number K840965.

Who is the listed applicant for SITE COAXIAL I/A HANDPIECE 30 TIP?

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

What is the FDA product code for SITE COAXIAL I/A HANDPIECE 30 TIP?

The FDA product code for SITE COAXIAL I/A HANDPIECE 30 TIP is HQC.

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Related Devices (Code: HQC)

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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.