FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

JM-102 JAUNDICE METER

K Number: K972309 · Decision Sep 22, 1998
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
16
Applicant Total
33
Review Days
459

Basic Information

Device Name
JM-102 JAUNDICE METER
K Number
K972309
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1113
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AIR-SHIELDS, INC.
Date Received
June 20, 1997
Decision Date
September 22, 1998
Product Code
MQM
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
MQM Bilirubin (Total And Unbound) In The Neonate Test System

Similar 510(k) Clearances

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

View all

Other Clearances by AIR-SHIELDS, INC.

K Number Device Name
K974248 WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM
K971256 DUO-LITE PHOTOTHERAPY SYSTEM
K960980 ISOLETTE INFANT INCUBATOR
K924709 SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETE
K940951 RW RESUCITAIRE INFANT RADIANT WARMER
K940975 C450/C400 INFANT INCUBATORS
K941106 MODEL TI500 ISOLETTE INFANT INCUBATOR
K924170 ISOLETTE INCUBATOR HUMIDITY METER
K922150 EXAMINATION LAMP
K914864 MODELS C500/C550 ISOLETE(R) INFANT INCUBATOR
Search all 33 clearances from AIR-SHIELDS, INC. →