PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T
K-Number: K062605 · 2006-11-09
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Device Summary
Frequently Asked Questions
What is the PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T?
PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T is a medical device that received FDA 510(k) clearance on 2006-11-09. The listed applicant is Philips Medical Systems. The 510(k) number is K062605.
When did PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T receive FDA 510(k) clearance?
PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T received FDA 510(k) clearance on 2006-11-09, under 510(k) number K062605.
Who is the listed applicant for PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T?
The FDA 510(k) record lists Philips Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T?
The FDA product code for PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T 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 Philips Medical Systems 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.
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.
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