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FDA 510(k)

VITALSAT PULSE OXIMETER, MODEL IC32000

K-Number: K011365 · 2001-10-26

Decision Date2001-10-26
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALSAT PULSE OXIMETER, MODEL IC32000 is the device name listed in this FDA 510(k) record. The listed applicant is Island Critical Care Corp.. It received FDA 510(k) clearance on 2001-10-26 under 510(k) number K011365. 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 VITALSAT PULSE OXIMETER, MODEL IC32000?

VITALSAT PULSE OXIMETER, MODEL IC32000 is a medical device that received FDA 510(k) clearance on 2001-10-26. The listed applicant is Island Critical Care Corp.. The 510(k) number is K011365.

When did VITALSAT PULSE OXIMETER, MODEL IC32000 receive FDA 510(k) clearance?

VITALSAT PULSE OXIMETER, MODEL IC32000 received FDA 510(k) clearance on 2001-10-26, under 510(k) number K011365.

Who is the listed applicant for VITALSAT PULSE OXIMETER, MODEL IC32000?

The FDA 510(k) record lists Island Critical Care Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITALSAT PULSE OXIMETER, MODEL IC32000?

The FDA product code for VITALSAT PULSE OXIMETER, MODEL IC32000 is DQA.

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.

Related Devices (Code: DQA)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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