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FDA 510(k)

RE-BAG MULTI-USE POUCH, LARGE & SMALL

K-Number: K954185 · 1995-12-04

ApplicantMiltex, Inc.
Decision Date1995-12-04
Product CodeKCT
Advisory CommitteeHO
DecisionUnknown

Device Summary

RE-BAG MULTI-USE POUCH, LARGE & SMALL is the device name listed in this FDA 510(k) record. The listed applicant is Miltex, Inc.. It received FDA 510(k) clearance on 1995-12-04 under 510(k) number K954185. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the RE-BAG MULTI-USE POUCH, LARGE & SMALL?

RE-BAG MULTI-USE POUCH, LARGE & SMALL is a medical device that received FDA 510(k) clearance on 1995-12-04. The listed applicant is Miltex, Inc.. The 510(k) number is K954185.

When did RE-BAG MULTI-USE POUCH, LARGE & SMALL receive FDA 510(k) clearance?

RE-BAG MULTI-USE POUCH, LARGE & SMALL received FDA 510(k) clearance on 1995-12-04, under 510(k) number K954185.

Who is the listed applicant for RE-BAG MULTI-USE POUCH, LARGE & SMALL?

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

What is the FDA product code for RE-BAG MULTI-USE POUCH, LARGE & SMALL?

The FDA product code for RE-BAG MULTI-USE POUCH, LARGE & SMALL is KCT.

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Related Devices (Code: KCT)

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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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