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)

MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER

K-Number: K872138 · 1987-10-07

ApplicantFisher & Paykel Allied Products , Ltd.
Decision Date1987-10-07
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Allied Products , Ltd.. It received FDA 510(k) clearance on 1987-10-07 under 510(k) number K872138. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER?

MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1987-10-07. The listed applicant is Fisher & Paykel Allied Products , Ltd.. The 510(k) number is K872138.

When did MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER receive FDA 510(k) clearance?

MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER received FDA 510(k) clearance on 1987-10-07, under 510(k) number K872138.

Who is the listed applicant for MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER?

The FDA 510(k) record lists Fisher & Paykel Allied Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER?

The FDA product code for MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER is BTT.

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 Fisher & Paykel Allied Products , 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.

K880702MODEL MR430 SPECIAL PURPOSE HUMID. HEATER BASESK872139MR420 TRANSPORT HUMIDIFIERK863377MR338 SERVO HEATED DELIVERY HUMIDIFIERK870055MR590 DUAL HOSE HEATER POWER PACKK862923MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIERK852962PERIPHERAL NERVE STIMULATOR MODEL A400

View all 12 devices →

Related Devices (Code: BTT)

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.

K262268Optiflow Oxygen Kit (AA484J)Fisher and Paykel Healthcare LimitedK254078HVT 2.0Vapotherm, Inc.K251448FL-10000U Respiratory HumidifierFlexicare Medical Limited.K251419Laboratorios Biogalenic Sterile Water for Inhalation, USPLaboratorios Biogalenic S.A. DE C.V.K253479Optiflow Switch+ Filtered Nasal Interface with CO2 Sampling (AA042J)Fisher & Paykel Healthcare, Ltd.K250312Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus and Soft Plus Cannula Extra SmallMedline Industries, LP

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.

↑