FDA UDI Not in Commercial Distribution 🇺🇸 United States

Footswitch

DI: 00817495021133 · Model: 5103-00-0030 · Candela Corporation
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Footswitch
Primary DI
00817495021133
Version / Model
5103-00-0030
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
9
Public Version Date
2023-12-20
Public Version Status
Update
Public Device Record Key
d1f98bcd-b101-48f5-935f-163d67102ae5
Distribution End Date
2023-12-19

Device Description

Footswitch

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
57890 Dermatological dye laser system
47877 Dermatological frequency-doubled solid-state laser system

Identifiers

Type ID
Primary 00817495021133

Premarket Submissions

Submission Number Supplement Number
K081324 000
K140122 000
K140732 000
K220853 000
K230990 000