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FDA 510(k)

CLAY-PARK LABS, INC. - LUBRICATING JELLY

K-Number: K012203 · 2001-08-27

ApplicantClay-Park Labs, Inc.
Decision Date2001-08-27
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CLAY-PARK LABS, INC. - LUBRICATING JELLY is the device name listed in this FDA 510(k) record. The listed applicant is Clay-Park Labs, Inc.. It received FDA 510(k) clearance on 2001-08-27 under 510(k) number K012203. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAY-PARK LABS, INC. - LUBRICATING JELLY?

CLAY-PARK LABS, INC. - LUBRICATING JELLY is a medical device that received FDA 510(k) clearance on 2001-08-27. The listed applicant is Clay-Park Labs, Inc.. The 510(k) number is K012203.

When did CLAY-PARK LABS, INC. - LUBRICATING JELLY receive FDA 510(k) clearance?

CLAY-PARK LABS, INC. - LUBRICATING JELLY received FDA 510(k) clearance on 2001-08-27, under 510(k) number K012203.

Who is the listed applicant for CLAY-PARK LABS, INC. - LUBRICATING JELLY?

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

What is the FDA product code for CLAY-PARK LABS, INC. - LUBRICATING JELLY?

The FDA product code for CLAY-PARK LABS, INC. - LUBRICATING JELLY is NUC.

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Related Devices (Code: NUC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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