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

EXAMINATION LAMP

K Number: K922150 · Decision Jul 21, 1992
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
36
Applicant Total
33
Review Days
75

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Basic Information

Device Name
EXAMINATION LAMP
K Number
K922150
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6320
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Air-Shields, Inc.
Date Received
May 7, 1992
Decision Date
July 21, 1992
Product Code
KZF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KZF Device, Medical Examination, Ac Powered

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Other Clearances by Air-Shields, Inc.

K Number Device Name
K974248 WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM
K972309 JM-102 JAUNDICE METER
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
K914864 MODELS C500/C550 ISOLETE(R) INFANT INCUBATOR
Search all 33 clearances from Air-Shields, Inc. →