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FDA 510(k)

PROTOUCH OVERGLOVE

K-Number: K952241 · 1995-08-07

ApplicantCottrell, Ltd.
Decision Date1995-08-07
Product CodeMMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROTOUCH OVERGLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Cottrell, Ltd.. It received FDA 510(k) clearance on 1995-08-07 under 510(k) number K952241. The device is classified under product code MMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTOUCH OVERGLOVE?

PROTOUCH OVERGLOVE is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is Cottrell, Ltd.. The 510(k) number is K952241.

When did PROTOUCH OVERGLOVE receive FDA 510(k) clearance?

PROTOUCH OVERGLOVE received FDA 510(k) clearance on 1995-08-07, under 510(k) number K952241.

Who is the listed applicant for PROTOUCH OVERGLOVE?

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

What is the FDA product code for PROTOUCH OVERGLOVE?

The FDA product code for PROTOUCH OVERGLOVE is MMP.

Related Clinical Trials

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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Other records listing Cottrell, Ltd. as applicant

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.

K972708ENDO-SPOR PLUS / HYPROCIDEK970726VAPOCIDEK960089PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATORK952234BARRIER ALL FILMK932922PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATORK951983IMNI-II

View all 9 devices →

Related Devices (Code: MMP)

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.

K091178MTP DISPOSABLE EQUIPMENT COVERS, KARL STORZ 15 TOUCH SCREENMtp Medical Technical Promotion GmbHK043234LIGHT DRAPEWrapped IN ComfortK041501GUANGZHOU FORTUNIQUE DRAPES, BAGS AND COVERSGuangzhou Fortunique , Ltd.K040794INCUBATOR CAPEWrapped IN ComfortK032065MEDLINE BAND BAGS AND EQUIPMENT COVERSMedline Industries, Inc.K023540SNAP KOVER, MODEL 01-2020; SNAP KAPS, MODEL 03-KP09Valumed

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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