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FDA 510(k)

PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW.

K-Number: K896152 · 1990-01-09

ApplicantPuritan Bennett Corp.
Decision Date1990-01-09
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW. is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1990-01-09 under 510(k) number K896152. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW.?

PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW. is a medical device that received FDA 510(k) clearance on 1990-01-09. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K896152.

When did PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW. receive FDA 510(k) clearance?

PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW. received FDA 510(k) clearance on 1990-01-09, under 510(k) number K896152.

Who is the listed applicant for PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW.?

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

What is the FDA product code for PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW.?

The FDA product code for PURITAN-BENNETT OXYGEN PRESSURE REGULATOR W/FLOW. is CAN.

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Other records listing Puritan Bennett 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.

K063650VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840K053388MODEL 840 VENTILATOR WITH PROPORTIONAL ASSIST VENTILATION PLUS SOFTWARE OPTIONK023225PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWAREK022103PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEMK001646PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTIONK002001BREEZE SLEEPGEAR WITH DREAMSEAL

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Related Devices (Code: CAN)

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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., Inc.

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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