Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MODEL SB100II FINGER PULSE OXIMETER

K-Number: K101568 · 2010-09-20

ApplicantAtlantean
Decision Date2010-09-20
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL SB100II FINGER PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Atlantean. It received FDA 510(k) clearance on 2010-09-20 under 510(k) number K101568. 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 MODEL SB100II FINGER PULSE OXIMETER?

MODEL SB100II FINGER PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 2010-09-20. The listed applicant is Atlantean. The 510(k) number is K101568.

When did MODEL SB100II FINGER PULSE OXIMETER receive FDA 510(k) clearance?

MODEL SB100II FINGER PULSE OXIMETER received FDA 510(k) clearance on 2010-09-20, under 510(k) number K101568.

Who is the listed applicant for MODEL SB100II FINGER PULSE OXIMETER?

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

What is the FDA product code for MODEL SB100II FINGER PULSE OXIMETER?

The FDA product code for MODEL SB100II FINGER 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.

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

View on FDA Database →

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

↑