Medical Device Manufacturer · US , Walker , MI

Life Products, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1977

Total

Cleared

Denied

Life Products, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Walker, US.

Historical record: 10 cleared submissions from 1977 to 1990.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Life Products, Inc.

10 devices

1-10 of 10

Cleared Jun 27, 1990

LIFESTYLE HOME TANNING UNITS

K901714 · LEJ

General & Plastic Surgery · 75d

Cleared Dec 24, 1985

LPA-1 PRESSURE MONITOR

K854022

Cardiovascular · 85d

Cleared Jul 19, 1985

L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT

K850151 · BZO

Anesthesiology · 185d

Anesthesiology · 234d

L100D PATIENT CIRCUIT DUAL LINE

K844290 · BZO

Anesthesiology · 66d

Cleared Feb 01, 1977

MODEL LP-3 PORTABLE VOLUME VENTILATOR

K770132 · CBK

Anesthesiology · 11d

Life Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Life Products, Inc.

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