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

MEDIAID UNIVERSAL THERMOMETER

K Number: K941673 · Decision Aug 25, 1994
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
32
Applicant Total
16
Review Days
142

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Basic Information

Device Name
MEDIAID UNIVERSAL THERMOMETER
K Number
K941673
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2920
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Polymedica Industries, Inc.
Date Received
April 5, 1994
Decision Date
August 25, 1994
Product Code
FLK
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
FLK Thermometer, Clinical Mercury

Similar 510(k) Clearances

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Other Clearances by Polymedica Industries, Inc.

K Number Device Name
K964398 SPYROFLEX PIGMENTED WOUND DRESSING/SPYROFLEX WOUND DRESSING TINTED
K971045 BASIS FLEXIBLE TIP DIGITAL THERMOMETER
K964701 MITRAFLEX PIGMENTED WOUND DRESSING
K963623 SPYROFLEX PIGMENTED WOUND DRESSING
K962991 BASIS BABY-TEMP PACIFIER DIGITAL THEROMETER
K955383 SPYROCOLLOID WOUND DRESSING
K953885 SPYROFLEX SKIN PROTECTOR
K952756 MEDI-AID BASAL THERMOMETER
K952159 BASIS DIGITAL THERMOMETER
K953618 SPYROFLEX WOUND DRESSING
Search all 16 clearances from Polymedica Industries, Inc. →