FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02

K Number: K982619 · Decision Aug 12, 1998
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
119
Applicant Total
230
Review Days
16

Basic Information

Device Name
HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02
K Number
K982619
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HEWLETT-PACKARD CO.
Date Received
July 27, 1998
Decision Date
August 12, 1998
Product Code
CCL
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CCL), ordered by most recent decision date.

View all

Other Clearances by HEWLETT-PACKARD CO.

K Number Device Name
K992543 HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLE
K993587 HP M2376A DEVICE LINK SYSTEM
K993169 MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810A
K992977 HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504A
K993516 HP M2600A VIRIDIA TELEMETRY SYSTEM
K993171 HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A
K992636 HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A
K991871 HEWLETT PACKARD MULTI FUNCTION ADULT DEFIB ELECTRODE, MODEL M3501A & M3502A
K984194 HP M2376A DEVICE LINK SYSTEM
K990400 LINEAR ARRAY TRANSDUCER,MODEL HP 21376, M2410A ULTRASOUND IMAGING SYSTEM
Search all 230 clearances from HEWLETT-PACKARD CO. →