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FDA 510(k)

LSPI PRESSURE REGULATOR

K-Number: K936187 · 1994-01-27

ApplicantLife Support Products, Inc.
Decision Date1994-01-27
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LSPI PRESSURE REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Support Products, Inc.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K936187. 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 LSPI PRESSURE REGULATOR?

LSPI PRESSURE REGULATOR is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Life Support Products, Inc.. The 510(k) number is K936187.

When did LSPI PRESSURE REGULATOR receive FDA 510(k) clearance?

LSPI PRESSURE REGULATOR received FDA 510(k) clearance on 1994-01-27, under 510(k) number K936187.

Who is the listed applicant for LSPI PRESSURE REGULATOR?

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

What is the FDA product code for LSPI PRESSURE REGULATOR?

The FDA product code for LSPI PRESSURE REGULATOR is CAN.

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Other records listing Life Support Products, 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.

K941871LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100K941870LSPI AUTOMATIC VENTILATOR, MODEL AV2000-100K940934LIFE VACK922819INFANT DISPOSABLE BAG MASK RESUSCITATORK932199LSPI AUTOMATIC VENTILATOR, MODEL AV3000K922691LSP (MODEL 554) BAG MASK RESUSCITATOR

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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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