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

BASIS DIGITAL THERMOMETER

K Number: K952159 · Decision Sep 22, 1995
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
16
Review Days
137

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Basic Information

Device Name
BASIS DIGITAL THERMOMETER
K Number
K952159
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Polymedica Industries, Inc.
Date Received
May 8, 1995
Decision Date
September 22, 1995
Product Code
FLL
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
FLL Continuous Measurement Thermometer

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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
K953618 SPYROFLEX WOUND DRESSING
K951862 A GEL WOUND DRESSING
Search all 16 clearances from Polymedica Industries, Inc. →