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

MODEL J25-25 WATT CO2 LASER

K Number: K851425 · Decision Nov 12, 1985
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
47
Applicant Total
17
Review Days
216

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Basic Information

Device Name
MODEL J25-25 WATT CO2 LASER
K Number
K851425
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4550
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Britt Corp., Inc.
Date Received
April 10, 1985
Decision Date
November 12, 1985
Product Code
HHR
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HHR Laser, Surgical, Gynecologic

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Other Clearances by Britt Corp., Inc.

K Number Device Name
K003828 VASO PRESS DVT FOOT GARMENT #VP 520
K991038 VASO PRESS DVT SYSTEM, MODELS VP500, VP501
K974393 VASO PRESS SYSTEM
K860977 MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION
K860975 MODEL 545-45 LASER FOR EAR, NOSE & THROAT
K860974 MODEL 545-45 LASER FOR DERMA., POD., SURGICAL
K860277 MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT
K860273 MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY
K860278 MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTIC
K840020 FITNESS LOGGER
Search all 17 clearances from Britt Corp., Inc. →