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FDA 510(k)

STERRAD(R) 100NX STERILIZER DUO CYCLE

K-Number: K111377 · 2012-09-13

Decision Date2012-09-13
Product CodeMLR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERRAD(R) 100NX STERILIZER DUO CYCLE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Sterilization Products. It received FDA 510(k) clearance on 2012-09-13 under 510(k) number K111377. The device is classified under product code MLR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERRAD(R) 100NX STERILIZER DUO CYCLE?

STERRAD(R) 100NX STERILIZER DUO CYCLE is a medical device that received FDA 510(k) clearance on 2012-09-13. The listed applicant is Advanced Sterilization Products. The 510(k) number is K111377.

When did STERRAD(R) 100NX STERILIZER DUO CYCLE receive FDA 510(k) clearance?

STERRAD(R) 100NX STERILIZER DUO CYCLE received FDA 510(k) clearance on 2012-09-13, under 510(k) number K111377.

Who is the listed applicant for STERRAD(R) 100NX STERILIZER DUO CYCLE?

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

What is the FDA product code for STERRAD(R) 100NX STERILIZER DUO CYCLE?

The FDA product code for STERRAD(R) 100NX STERILIZER DUO CYCLE is MLR.

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.

Other records listing Advanced Sterilization Products 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.

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Related Devices (Code: MLR)

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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