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FDA 510(k)

MICRO-MITT

K-Number: K830821 · 1983-04-27

ApplicantCooperVision, Inc.
Decision Date1983-04-27
Product CodeFXP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO-MITT is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1983-04-27 under 510(k) number K830821. The device is classified under product code FXP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-MITT?

MICRO-MITT is a medical device that received FDA 510(k) clearance on 1983-04-27. The listed applicant is CooperVision, Inc.. The 510(k) number is K830821.

When did MICRO-MITT receive FDA 510(k) clearance?

MICRO-MITT received FDA 510(k) clearance on 1983-04-27, under 510(k) number K830821.

Who is the listed applicant for MICRO-MITT?

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 MICRO-MITT?

The FDA product code for MICRO-MITT is FXP.

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Related Devices (Code: FXP)

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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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