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FDA 510(k)

REPROCESSED PULSE OXIMETER SENSORS

K-Number: K102560 · 2011-02-18

ApplicantSterilmed, Inc.
Decision Date2011-02-18
Product CodeNLF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REPROCESSED PULSE OXIMETER SENSORS is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2011-02-18 under 510(k) number K102560. The device is classified under product code NLF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED PULSE OXIMETER SENSORS?

REPROCESSED PULSE OXIMETER SENSORS is a medical device that received FDA 510(k) clearance on 2011-02-18. The listed applicant is Sterilmed, Inc.. The 510(k) number is K102560.

When did REPROCESSED PULSE OXIMETER SENSORS receive FDA 510(k) clearance?

REPROCESSED PULSE OXIMETER SENSORS received FDA 510(k) clearance on 2011-02-18, under 510(k) number K102560.

Who is the listed applicant for REPROCESSED PULSE OXIMETER SENSORS?

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 PULSE OXIMETER SENSORS?

The FDA product code for REPROCESSED PULSE OXIMETER SENSORS is NLF.

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Related Devices (Code: NLF)

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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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