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FDA 510(k)

PRO BARRIER(TM) TUBE SOX(TM)

K-Number: K945575 · 1995-03-06

ApplicantCottrell, Ltd.
Decision Date1995-03-06
Product CodeMMN
DecisionSubstantially Equivalent

Device Summary

PRO BARRIER(TM) TUBE SOX(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Cottrell, Ltd.. It received FDA 510(k) clearance on 1995-03-06 under 510(k) number K945575. The device is classified under product code MMN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO BARRIER(TM) TUBE SOX(TM)?

PRO BARRIER(TM) TUBE SOX(TM) is a medical device that received FDA 510(k) clearance on 1995-03-06. The listed applicant is Cottrell, Ltd.. The 510(k) number is K945575.

When did PRO BARRIER(TM) TUBE SOX(TM) receive FDA 510(k) clearance?

PRO BARRIER(TM) TUBE SOX(TM) received FDA 510(k) clearance on 1995-03-06, under 510(k) number K945575.

Who is the listed applicant for PRO BARRIER(TM) TUBE SOX(TM)?

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 PRO BARRIER(TM) TUBE SOX(TM)?

The FDA product code for PRO BARRIER(TM) TUBE SOX(TM) is MMN.

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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 OVERGLOVEK952234BARRIER ALL FILMK932922PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR

View all 9 devices →

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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