Medical Device Manufacturer · US , Mchenry , IL

Warren E. Collins, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1978

Total

Cleared

Denied

Warren E. Collins, Inc. has 14 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1978 to 1994.

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 - Warren E. Collins, Inc.

14 devices

1-14 of 14

Cleared Feb 04, 1994

GS-MODULAR (GOLD STANDARD - MODULAR)

K925459 · BZG

Anesthesiology · 463d

Cleared Jan 15, 1992

COLLINS DIGITAL PULMONARY MANOMETER

K912946 · BXR

Anesthesiology · 194d

COLLINS PNEUMOTACH PFT SYSTEM

K861227 · BZG

Anesthesiology · 65d

Cleared Jul 31, 1985

COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM

K852102 · CCM

Anesthesiology · 77d

Cleared Sep 12, 1983

METABOLIC EXERCISE TESTING SYSTEM

K831780 · BZL

Anesthesiology · 102d

RS-RESIDUAL VOLUME SYSTEM

APEXLINE OF PULMONARY FUNCT. INSTRUM.

K803053 · BTY

Anesthesiology · 20d

Cleared Dec 22, 1980

SHELL KRATON THERMO-PLASTIC RUBBER COMP.

Physical Medicine · 15d

Cleared May 16, 1978

PULMONARY FUNCTION TESTER

K780584 · BTY

Anesthesiology · 35d

Cleared Mar 14, 1978

PULMONARY FUNCTION TESTER, COMPUTERIZED

K780328 · BZC

Anesthesiology · 15d

Warren E. Collins, Inc. - FDA 510(k) Cleared Devices

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