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FDA 510(k)

PERMALID PAK

K-Number: K842781 · 1985-08-01

ApplicantCooperVision, Inc.
Decision Date1985-08-01
Product Code
DecisionUnknown

Device Summary

PERMALID PAK is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1985-08-01 under 510(k) number K842781. FDA Decision: Unknown.

Frequently Asked Questions

What is the PERMALID PAK?

PERMALID PAK is a medical device that received FDA 510(k) clearance on 1985-08-01. The listed applicant is CooperVision, Inc.. The 510(k) number is K842781.

When did PERMALID PAK receive FDA 510(k) clearance?

PERMALID PAK received FDA 510(k) clearance on 1985-08-01, under 510(k) number K842781.

Who is the listed applicant for PERMALID PAK?

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

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Other records listing CooperVision, Inc. as applicant

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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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