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FDA 510(k)

CLAYMAN-PAREL CAPSULE COUPEUR

K-Number: K841101 · 1984-05-16

ApplicantMiami Eye Technology, Inc.
Decision Date1984-05-16
Product CodeHNY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CLAYMAN-PAREL CAPSULE COUPEUR is the device name listed in this FDA 510(k) record. The listed applicant is Miami Eye Technology, Inc.. It received FDA 510(k) clearance on 1984-05-16 under 510(k) number K841101. The device is classified under product code HNY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAYMAN-PAREL CAPSULE COUPEUR?

CLAYMAN-PAREL CAPSULE COUPEUR is a medical device that received FDA 510(k) clearance on 1984-05-16. The listed applicant is Miami Eye Technology, Inc.. The 510(k) number is K841101.

When did CLAYMAN-PAREL CAPSULE COUPEUR receive FDA 510(k) clearance?

CLAYMAN-PAREL CAPSULE COUPEUR received FDA 510(k) clearance on 1984-05-16, under 510(k) number K841101.

Who is the listed applicant for CLAYMAN-PAREL CAPSULE COUPEUR?

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

What is the FDA product code for CLAYMAN-PAREL CAPSULE COUPEUR?

The FDA product code for CLAYMAN-PAREL CAPSULE COUPEUR is HNY.

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Related Devices (Code: HNY)

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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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