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FDA 510(k)

Vis-U-All Low Temperature Sterilization Pouch/Tubing

K-Number: K172749 · 2018-02-09

Decision Date2018-02-09
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vis-U-All Low Temperature Sterilization Pouch/Tubing is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2018-02-09 under 510(k) number K172749. 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 Vis-U-All Low Temperature Sterilization Pouch/Tubing?

Vis-U-All Low Temperature Sterilization Pouch/Tubing is a medical device that received FDA 510(k) clearance on 2018-02-09. The listed applicant is STERIS Corporation. The 510(k) number is K172749.

When did Vis-U-All Low Temperature Sterilization Pouch/Tubing receive FDA 510(k) clearance?

Vis-U-All Low Temperature Sterilization Pouch/Tubing received FDA 510(k) clearance on 2018-02-09, under 510(k) number K172749.

Who is the listed applicant for Vis-U-All Low Temperature Sterilization Pouch/Tubing?

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

What is the FDA product code for Vis-U-All Low Temperature Sterilization Pouch/Tubing?

The FDA product code for Vis-U-All Low Temperature Sterilization Pouch/Tubing is FRG.

Other records listing STERIS Corporation 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.

View all 139 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.