FDA 510(k)

IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE

K-Number: K921607 · 1992-06-30

Decision Date1992-06-30

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE 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 1992-06-30 under 510(k) number K921607. 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 IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE?

IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE is a medical device that received FDA 510(k) clearance on 1992-06-30. The listed applicant is Chiron Vision Corp.. The 510(k) number is K921607.

When did IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE receive FDA 510(k) clearance?

IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE received FDA 510(k) clearance on 1992-06-30, under 510(k) number K921607.

Who is the listed applicant for IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE?

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 IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE?

The FDA product code for IOLAB REUSABLE PERISTATIC CASSETTE/OPHTHALMIC USE is 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.