RE-USABLE STERILIZATION POUCH / BAG
K-Number: K013715 · 2002-04-01
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Device Summary
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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