Intertech Resources, Inc. - FDA 510(k) Cleared Devices
29
Total
27
Cleared
0
Denied
Intertech Resources, Inc. has 27 FDA 510(k) cleared anesthesiology devices. Based in Fort Myers, US.
Historical record: 27 cleared submissions from 1987 to 1996.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
29 devices
Cleared
Dec 17, 1996
1ST RESPONSE DISPOSABLE MANOMETER
Anesthesiology
256d
Cleared
Jan 30, 1996
HEAT & MOISTURE EXCHANGER
Anesthesiology
90d
Cleared
Sep 15, 1995
HEAT MOISTURE EXCHANGER
Anesthesiology
45d
Cleared
Aug 11, 1995
XENON GAS BREATHING CIRCUIT
Radiology
91d
Cleared
Jun 08, 1995
PFT FILTER
General Hospital
37d
Cleared
Jun 08, 1995
SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC
Anesthesiology
31d
Cleared
Jun 08, 1995
SIMS INTERTECH HYPERINFLATION BAG SYSTEM
Anesthesiology
28d
Cleared
Jan 25, 1994
HEPA FILTERED HEAT AND MOISTURE EXCHANGER
Anesthesiology
118d
Cleared
Jul 01, 1993
HEPA FILTERED HME
General Hospital
134d
Cleared
Oct 30, 1992
DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIED
Anesthesiology
157d
Cleared
Jun 30, 1992
DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS
Anesthesiology
85d
Cleared
Oct 23, 1991
DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED
Anesthesiology
180d