STERRAD 100NX STERILIZER
K-Number: K071385 · 2007-11-29
Advertisement
Device Summary
Frequently Asked Questions
What is the STERRAD 100NX STERILIZER?
STERRAD 100NX STERILIZER is a medical device that received FDA 510(k) clearance on 2007-11-29. The listed applicant is Advanced Sterilization Products. The 510(k) number is K071385.
When did STERRAD 100NX STERILIZER receive FDA 510(k) clearance?
STERRAD 100NX STERILIZER received FDA 510(k) clearance on 2007-11-29, under 510(k) number K071385.
Who is the listed applicant for STERRAD 100NX STERILIZER?
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 100NX STERILIZER?
The FDA product code for STERRAD 100NX STERILIZER 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement