FDA 510(k)

FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2

K-Number: K061191 · 2006-05-22

Decision Date2006-05-22

Product CodeDQA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2 is the device name listed in this FDA 510(k) record. The listed applicant is Measurement Specialties, Inc.. It received FDA 510(k) clearance on 2006-05-22 under 510(k) number K061191. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2?

FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2 is a medical device that received FDA 510(k) clearance on 2006-05-22. The listed applicant is Measurement Specialties, Inc.. The 510(k) number is K061191.

When did FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2 receive FDA 510(k) clearance?

FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2 received FDA 510(k) clearance on 2006-05-22, under 510(k) number K061191.

Who is the listed applicant for FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2?

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

What is the FDA product code for FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2?

The FDA product code for FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2 is DQA.

Related Clinical Trials

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Related Devices (Code: DQA)

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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.