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)

RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.)

K-Number: K902276 · 1990-08-17

ApplicantRespironics, Inc.
Decision Date1990-08-17
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.) is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1990-08-17 under 510(k) number K902276. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.)?

RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.) is a medical device that received FDA 510(k) clearance on 1990-08-17. The listed applicant is Respironics, Inc.. The 510(k) number is K902276.

When did RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.) receive FDA 510(k) clearance?

RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.) received FDA 510(k) clearance on 1990-08-17, under 510(k) number K902276.

Who is the listed applicant for RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.)?

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

What is the FDA product code for RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.)?

The FDA product code for RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.) is CAP.

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 Respironics, 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.

K261262Altis Full Face MaskK243394AF531 Oro-Nasal SE Face MaskK231313Therapy Mask 3100 NC/SPK210844DreamWear Silicone Pillows MaskK210386Magneto Nasal MaskK202142Sleepware G3

View all 166 devices →

Related Devices (Code: CAP)

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.

K201666SINGLE USE MANOMETERFlexicare Medical Limited.K182292VORTRAN APM-PlusVortran Medical Technology 1, Inc.K180510NS 120P-TRS Airway Pressure GaugeInstrumentation Industries, Inc.K172284NAPA LP-15 Airway Pressure MonitorDrw Medical, LLCK153733VORTRAN ManometerVortran Medical Technology 1, Inc.K122627GIO DIGITAL PRESSURE GUAGESGalemed Corp.

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.

↑