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FDA 510(k)

LINEN (HUCK) TOWEL

K-Number: K865094 · 1987-01-20

ApplicantThe Eye Co-Op, Inc.
Decision Date1987-01-20
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LINEN (HUCK) TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is The Eye Co-Op, Inc.. It received FDA 510(k) clearance on 1987-01-20 under 510(k) number K865094. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINEN (HUCK) TOWEL?

LINEN (HUCK) TOWEL is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is The Eye Co-Op, Inc.. The 510(k) number is K865094.

When did LINEN (HUCK) TOWEL receive FDA 510(k) clearance?

LINEN (HUCK) TOWEL received FDA 510(k) clearance on 1987-01-20, under 510(k) number K865094.

Who is the listed applicant for LINEN (HUCK) TOWEL?

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

What is the FDA product code for LINEN (HUCK) TOWEL?

The FDA product code for LINEN (HUCK) TOWEL is KKX.

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Related Devices (Code: KKX)

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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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