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FDA 510(k)

SATLITE TRANS PORTABLE PULSE OXIMETER

K-Number: K890753 · 1989-03-22

Decision Date1989-03-22
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SATLITE TRANS PORTABLE PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Datex Division Instrumentarium Corp.. It received FDA 510(k) clearance on 1989-03-22 under 510(k) number K890753. 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 SATLITE TRANS PORTABLE PULSE OXIMETER?

SATLITE TRANS PORTABLE PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K890753.

When did SATLITE TRANS PORTABLE PULSE OXIMETER receive FDA 510(k) clearance?

SATLITE TRANS PORTABLE PULSE OXIMETER received FDA 510(k) clearance on 1989-03-22, under 510(k) number K890753.

Who is the listed applicant for SATLITE TRANS PORTABLE PULSE OXIMETER?

The FDA 510(k) record lists Datex Division Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SATLITE TRANS PORTABLE PULSE OXIMETER?

The FDA product code for SATLITE TRANS PORTABLE PULSE OXIMETER 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.

Other records listing Datex Division Instrumentarium Corp. as applicant

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.

View all 55 devices →

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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