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

GUARDIAN SAFE BOW

K Number: K901958 · Decision Jul 30, 1990
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
35
Applicant Total
14
Review Days
90

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Basic Information

Device Name
GUARDIAN SAFE BOW
K Number
K901958
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5500
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Lancer Orthodontics, Inc.
Date Received
May 1, 1990
Decision Date
July 30, 1990
Product Code
DZB
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
DZB Headgear, Extraoral, Orthodontic

Similar 510(k) Clearances

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Other Clearances by Lancer Orthodontics, Inc.

K Number Device Name
K122069 STORM MINI SCREW
K071192 BLUGOO HD
K051552 O.A.S.I. SYSTEM
K991481 PARAGON
K904090 ORTHODONTIC BONDING ADHESIVE CONTROL
K904092 LANCER ORIGINAL, SIERRA, GENERAL PURPOSE
K904093 BUCCAL TUBE, BUCCAL ATTACHMENT
K904091 TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO
K904089 PERMA MESH
K904094 C.A.T.,SINTERLINE,NATURAL ARCH,MICROTWIN,BIOTORQUE
Search all 14 clearances from Lancer Orthodontics, Inc. →