Atlas FDA

KENTEMP

FDA 510(k) clearance K953465 · decided 1995-12-15

Clearance details

K-number
K953465
Device name
KENTEMP
Applicant
Kentron Health Care, Inc.
Decision
Substantially Equivalent
Date received
1995-07-24
Decision date
1995-12-15
Days to decision
144 days
Clearance type
Traditional
Product code
FLK
Device class
2
Regulation number
880.2920
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Hollywood, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
AMSINO CLINICAL THERMOMETER (K960185)Amsia Intl., Inc.1996-03-28
GERATHERM MERCUIRY FREE CLINICAL THERMOMETER (K960224)Rg Ent., Inc.1996-03-25
CLINICAL GLASS THERMOMETER (K942483)Makol Medical Instruments Corp.1995-03-28
MEDIAID UNIVERSAL THERMOMETER (K941673)Polymedica Industries, Inc.1994-08-25
AMG MED BRAND CLINICAL GLASS THERMOMETER (K940380)Amg Medical, Inc.1994-05-04
AMG MED BRAND CLINICAL GLASS THERMOMETER (K940394)Technolab Industries (Canada) , Ltd.1994-05-04
GUARDIAN AND ANDINO MODELS (K932991)Coltemp, Inc.1994-01-28
LORREX HEALTH PRODUCTS - CLINICAL MERCURY THERMOME (K923225)Lorrex Health Products1993-06-08
SIMPEX INC. ORAL AND RECTAL THERMOMETERS (K913793)Simpex, Inc.1991-12-30
MERCURY AND GLASS FEVER THERMOMETER (K911269)Steridyne Corp.1991-05-15
CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT (K902625)Liaoning-Usa Corp.1990-10-26
MASCOT THERMOTER (K903500)Mascot, Inc.1990-10-09

Recalls involving this device

No recalls on record reference this clearance.