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FDA 510(k)

APEX MEDICAL WIZARD SERIES CPAP MASK

K-Number: K103174 · 2011-05-06

ApplicantApex Medical Corp.
Decision Date2011-05-06
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

APEX MEDICAL WIZARD SERIES CPAP MASK is the device name listed in this FDA 510(k) record. The listed applicant is Apex Medical Corp.. It received FDA 510(k) clearance on 2011-05-06 under 510(k) number K103174. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX MEDICAL WIZARD SERIES CPAP MASK?

APEX MEDICAL WIZARD SERIES CPAP MASK is a medical device that received FDA 510(k) clearance on 2011-05-06. The listed applicant is Apex Medical Corp.. The 510(k) number is K103174.

When did APEX MEDICAL WIZARD SERIES CPAP MASK receive FDA 510(k) clearance?

APEX MEDICAL WIZARD SERIES CPAP MASK received FDA 510(k) clearance on 2011-05-06, under 510(k) number K103174.

Who is the listed applicant for APEX MEDICAL WIZARD SERIES CPAP MASK?

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

What is the FDA product code for APEX MEDICAL WIZARD SERIES CPAP MASK?

The FDA product code for APEX MEDICAL WIZARD SERIES CPAP MASK is BZD.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Apex Medical 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.

K213577VenAir, Sequential Compression SystemK193206WiZARD 510 Nasal MaskK182394WiZARD 310/320 Series CPAP MaskK121642WIZARD 230 NASAL PILOW MASKK112079APEX MEDICAL XT AUTO CPAP WITH COMPLIANCE IMPROVEMENT ALGORITHM 9S-005720K120035APEX MEDICAL ICH CPAP SERIES (9S-007XXX)

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Related Devices (Code: BZD)

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.

K261262Altis Full Face MaskRespironics, Inc.K253044RXiBreeze PAP System (RXiBreeze 20C)Resvent Medical Technology Co., Ltd.K253553OrionResmed CorpK254104ResScan EssentialsResmed CorpK251920Sleep Apnea Breathing Therapy Mask:JoyMask 20-B Full Face Mask, JoyMask 21-B Full Face MaskDcstar, Inc.K253166F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)BMC Medical Co., Ltd.

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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