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)

PULSE OXIMETER ADAPTER CABLES

K-Number: K052544 · 2006-09-29

Decision Date2006-09-29
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PULSE OXIMETER ADAPTER CABLES is the device name listed in this FDA 510(k) record. The listed applicant is American I.V. Products, Inc.. It received FDA 510(k) clearance on 2006-09-29 under 510(k) number K052544. 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 PULSE OXIMETER ADAPTER CABLES?

PULSE OXIMETER ADAPTER CABLES is a medical device that received FDA 510(k) clearance on 2006-09-29. The listed applicant is American I.V. Products, Inc.. The 510(k) number is K052544.

When did PULSE OXIMETER ADAPTER CABLES receive FDA 510(k) clearance?

PULSE OXIMETER ADAPTER CABLES received FDA 510(k) clearance on 2006-09-29, under 510(k) number K052544.

Who is the listed applicant for PULSE OXIMETER ADAPTER CABLES?

The FDA 510(k) record lists American I.V. Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULSE OXIMETER ADAPTER CABLES?

The FDA product code for PULSE OXIMETER ADAPTER CABLES 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 American I.V. Products, Inc. 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 7 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

View on FDA Database →

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

↑