Medical Device Manufacturer · US , Walker , MI

Palco Laboratories, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1983

Total

Cleared

Denied

Palco Laboratories, Inc. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1983 to 1995. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Palco Laboratories, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Palco Laboratories, Inc.

9 devices

1-9 of 9

Cleared Jun 28, 1995

PALCO LABS COLD POUCH

K942810 · LDQ

General & Plastic Surgery · 378d

Cleared Mar 24, 1995

PULSE OXIMETER MODEL 305

K943842 · DQA

Anesthesiology · 231d

Cleared Mar 16, 1993

PALCO LABS MODEL 340 PULSE OXIMETER

K920066 · DQA

Anesthesiology · 434d

Cleared Dec 17, 1991

PALCO LABS LOADMATIC

K913694 · FMF

General Hospital · 120d

Cleared Jun 10, 1991

PALCO LABS MODEL 300 OXYGEN/PULSE MONITOR

K911191 · DQA

Anesthesiology · 84d

Cleared Mar 18, 1991

PALCO LABS MODEL 400 OXYGEN/PULSE MONITOR

K904988 · DQA

Anesthesiology · 131d

Cleared Sep 04, 1987

INJECT-EASE

K872233 · KZH

General Hospital · 86d

Cleared Oct 19, 1984

WET-STOP

K842547 · KPN

Gastroenterology & Urology · 109d

Cleared Nov 07, 1983

AUTO-LANCET

K833344 · FMK

General & Plastic Surgery · 41d

Palco Laboratories, Inc. - FDA 510(k) Cleared Devices

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