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 PTL REVIVEEASY

K-Number: K863172 · 1986-11-04

ApplicantRespironics, Inc.
Decision Date1986-11-04
Product CodeCAO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRONICS PTL REVIVEEASY is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1986-11-04 under 510(k) number K863172. The device is classified under product code CAO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRONICS PTL REVIVEEASY?

RESPIRONICS PTL REVIVEEASY is a medical device that received FDA 510(k) clearance on 1986-11-04. The listed applicant is Respironics, Inc.. The 510(k) number is K863172.

When did RESPIRONICS PTL REVIVEEASY receive FDA 510(k) clearance?

RESPIRONICS PTL REVIVEEASY received FDA 510(k) clearance on 1986-11-04, under 510(k) number K863172.

Who is the listed applicant for RESPIRONICS PTL REVIVEEASY?

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 PTL REVIVEEASY?

The FDA product code for RESPIRONICS PTL REVIVEEASY is CAO.

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: CAO)

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.

K971348FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEMGreen Field Medical Sourcing, Inc.K894032EVAC-TUBESharn, Inc.K875226ESOPHAGEAL OBTURATOR/TRACHEAL TUBESheridan Catheter Corp.K864200VETA/VENTED ESOPHAGEAL TUBE AIRWAYCranco Co.K761195ESOPHAGEAL OBTURATION AIRWAYMckesson 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.

↑