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FDA 510(k)

BARRIER ALL FILM

K-Number: K952234 · 1995-07-31

ApplicantCottrell, Ltd.
Decision Date1995-07-31
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BARRIER ALL FILM is the device name listed in this FDA 510(k) record. The listed applicant is Cottrell, Ltd.. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K952234. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRIER ALL FILM?

BARRIER ALL FILM is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Cottrell, Ltd.. The 510(k) number is K952234.

When did BARRIER ALL FILM receive FDA 510(k) clearance?

BARRIER ALL FILM received FDA 510(k) clearance on 1995-07-31, under 510(k) number K952234.

Who is the listed applicant for BARRIER ALL FILM?

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 BARRIER ALL FILM?

The FDA product code for BARRIER ALL FILM is EFS.

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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 INDICATORK952241PROTOUCH OVERGLOVEK932922PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATORK951983IMNI-II

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Related Devices (Code: EFS)

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.

K023232SPLATRFREE SWANGLE 360 DISPOSABLE PROPHYLAXIS ANGLESmartpracticeK001493DENTAL AIR FORCE HOME DENTAL CLEANING SYSTEM, MODEL NO. 0020001Air Force, Inc.K983374AGATHA-A-H2010Midian Intl.K964810DERMADAMUltradent Products, Inc.K943182ORAL-B PERIOFLEX SUBGINGIVAL IRRIGATOROral-B LaboratoriesK923711PERIOFLEX TIPNovadent, Ltd.

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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