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FDA 510(k)

INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE

K-Number: K890300 · 1989-04-17

ApplicantCooperVision, Inc.
Decision Date1989-04-17
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1989-04-17 under 510(k) number K890300. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE?

INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is CooperVision, Inc.. The 510(k) number is K890300.

When did INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE receive FDA 510(k) clearance?

INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE received FDA 510(k) clearance on 1989-04-17, under 510(k) number K890300.

Who is the listed applicant for INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE?

The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE?

The FDA product code for INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE is HQE.

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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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