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FDA 510(k)

RE-USABLE STERILIZATION POUCH / BAG

K-Number: K013715 · 2002-04-01

Decision Date2002-04-01
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RE-USABLE STERILIZATION POUCH / BAG is the device name listed in this FDA 510(k) record. The listed applicant is Quality Products of Montana. It received FDA 510(k) clearance on 2002-04-01 under 510(k) number K013715. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RE-USABLE STERILIZATION POUCH / BAG?

RE-USABLE STERILIZATION POUCH / BAG is a medical device that received FDA 510(k) clearance on 2002-04-01. The listed applicant is Quality Products of Montana. The 510(k) number is K013715.

When did RE-USABLE STERILIZATION POUCH / BAG receive FDA 510(k) clearance?

RE-USABLE STERILIZATION POUCH / BAG received FDA 510(k) clearance on 2002-04-01, under 510(k) number K013715.

Who is the listed applicant for RE-USABLE STERILIZATION POUCH / BAG?

The FDA 510(k) record lists Quality Products of Montana as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RE-USABLE STERILIZATION POUCH / BAG?

The FDA product code for RE-USABLE STERILIZATION POUCH / BAG is FRG.

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.

Related Devices (Code: FRG)

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.

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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