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FDA 510(k)

MED-TEC REDI-FOAM

K-Number: K951808 · 1995-07-06

ApplicantMedtec, Inc.
Decision Date1995-07-06
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MED-TEC REDI-FOAM is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1995-07-06 under 510(k) number K951808. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-TEC REDI-FOAM?

MED-TEC REDI-FOAM is a medical device that received FDA 510(k) clearance on 1995-07-06. The listed applicant is Medtec, Inc.. The 510(k) number is K951808.

When did MED-TEC REDI-FOAM receive FDA 510(k) clearance?

MED-TEC REDI-FOAM received FDA 510(k) clearance on 1995-07-06, under 510(k) number K951808.

Who is the listed applicant for MED-TEC REDI-FOAM?

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

What is the FDA product code for MED-TEC REDI-FOAM?

The FDA product code for MED-TEC REDI-FOAM is IYE.

Other records listing Medtec, Inc. as applicant

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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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