DUAL HEATED INFANT VREATHING CIROUITS
K-Number: K103767 · 2012-04-16
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Device Summary
Frequently Asked Questions
What is the DUAL HEATED INFANT VREATHING CIROUITS?
DUAL HEATED INFANT VREATHING CIROUITS is a medical device that received FDA 510(k) clearance on 2012-04-16. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K103767.
When did DUAL HEATED INFANT VREATHING CIROUITS receive FDA 510(k) clearance?
DUAL HEATED INFANT VREATHING CIROUITS received FDA 510(k) clearance on 2012-04-16, under 510(k) number K103767.
Who is the listed applicant for DUAL HEATED INFANT VREATHING CIROUITS?
The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUAL HEATED INFANT VREATHING CIROUITS?
The FDA product code for DUAL HEATED INFANT VREATHING CIROUITS is BZE.
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 Fisher & Paykel Healthcare, Ltd. 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: BZE)
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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