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FDA 510(k)

VANGUARD REPROCESSED PULSE OXIMETER SENSORS

K-Number: K012344 · 2002-10-04

ApplicantVanguard Medical Concepts, Inc.
Decision Date2002-10-04
Product CodeNLF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VANGUARD REPROCESSED PULSE OXIMETER SENSORS is the device name listed in this FDA 510(k) record. The listed applicant is Vanguard Medical Concepts, Inc.. It received FDA 510(k) clearance on 2002-10-04 under 510(k) number K012344. 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 VANGUARD REPROCESSED PULSE OXIMETER SENSORS?

VANGUARD REPROCESSED PULSE OXIMETER SENSORS is a medical device that received FDA 510(k) clearance on 2002-10-04. The listed applicant is Vanguard Medical Concepts, Inc.. The 510(k) number is K012344.

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

VANGUARD REPROCESSED PULSE OXIMETER SENSORS received FDA 510(k) clearance on 2002-10-04, under 510(k) number K012344.

Who is the listed applicant for VANGUARD REPROCESSED PULSE OXIMETER SENSORS?

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

What is the FDA product code for VANGUARD REPROCESSED PULSE OXIMETER SENSORS?

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

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Related Devices (Code: NLF)

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.

K241758Reprocessed RD SET Adt Pulse Oximeter Sensor (4000); Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001); Reprocessed RD SET Inf Pulse Oximeter Sensor (4002); Reprocessed RD SET Adt Pulse Oximeter Sensor (4003)Stryker Sustainability SolutionsK222019Reprocessed RD SET Adt Pulse Oximeter Sensor (4000), Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001), Reprocessed RD SET Inf Pulse Oximeter Sensor (4002), Reprocessed RD SET Adt Pulse Oximeter Sensor (4003)Stryker Sustainability SolutionsK211138Reprocessed Pulse Oximeter Sensor (D-25), Reprocessed Pulse Oximeter Sensor (D-25L), Reprocessed Pulse Oximeter Sensor (D-20), Reprocessed Pulse Oximeter Sensor (N-25), Reprocessed Pulse Oximeter Sensor (I-20), Reprocessed Pulse Oximeter Sensor (Max-A), Reprocessed Pulse Oximeter Sensor (Max-AL), Reprocessed Pulse Oximeter Sensor (Max-P), Reprocessed Pulse Oximeter Sensor (Max-N), Reprocessed Pulse Oximeter Sensor (Max-I)Stryker Sustainability SolutionsK201699Medline ReNewal Reprocessed Nellcor OxiMax SpO2 SensorSurgical Instrument and Savings Inc (Dba Medline Renewal)K191018Medline ReNewal Reprocessed Masimo LNCS Series Adult and Pediatric SpO2 Adhesive SensorsSurgical Instrument Service and Savings, Inc.K111773RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATERenu Medical, Inc.

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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