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FDA 510(k)

STERIKING STERILIZATION POUCHES & ROLLS

K-Number: K953776 · 1995-10-12

ApplicantWihuri OY
Decision Date1995-10-12
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERIKING STERILIZATION POUCHES & ROLLS is the device name listed in this FDA 510(k) record. The listed applicant is Wihuri OY. It received FDA 510(k) clearance on 1995-10-12 under 510(k) number K953776. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERIKING STERILIZATION POUCHES & ROLLS?

STERIKING STERILIZATION POUCHES & ROLLS is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is Wihuri OY. The 510(k) number is K953776.

When did STERIKING STERILIZATION POUCHES & ROLLS receive FDA 510(k) clearance?

STERIKING STERILIZATION POUCHES & ROLLS received FDA 510(k) clearance on 1995-10-12, under 510(k) number K953776.

Who is the listed applicant for STERIKING STERILIZATION POUCHES & ROLLS?

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

What is the FDA product code for STERIKING STERILIZATION POUCHES & ROLLS?

The FDA product code for STERIKING STERILIZATION POUCHES & ROLLS is KCT.

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: KCT)

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.

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