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

DISPOSABLE LARYNGOSCOPE

K Number: K850437 · Decision Feb 14, 1985
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
75
Review Days
9

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Basic Information

Device Name
DISPOSABLE LARYNGOSCOPE
K Number
K850437
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4550
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Vital Signs, Inc.
Date Received
February 5, 1985
Decision Date
February 14, 1985
Product Code
LLW
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
LLW Laser, Neodymium:Yag For Gynecologic Use

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K994044 CLEEN-ABLE
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