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FDA 510(k)

REPROCESSED SCISSOR TIPS

K-Number: K073613 · 2008-02-12

ApplicantSterilmed, Inc.
Decision Date2008-02-12
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED SCISSOR TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2008-02-12 under 510(k) number K073613. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED SCISSOR TIPS?

REPROCESSED SCISSOR TIPS is a medical device that received FDA 510(k) clearance on 2008-02-12. The listed applicant is Sterilmed, Inc.. The 510(k) number is K073613.

When did REPROCESSED SCISSOR TIPS receive FDA 510(k) clearance?

REPROCESSED SCISSOR TIPS received FDA 510(k) clearance on 2008-02-12, under 510(k) number K073613.

Who is the listed applicant for REPROCESSED SCISSOR TIPS?

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

What is the FDA product code for REPROCESSED SCISSOR TIPS?

The FDA product code for REPROCESSED SCISSOR TIPS is NUJ.

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Related Devices (Code: NUJ)

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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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