Medical Bio Care Sweden AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Bio Care Sweden AB - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Medical Bio Care Sweden AB has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Albuquerque,, US.
Historical record: 10 cleared submissions from 2000 to 2002.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Bio Care Sweden AB
10 devices
Cleared
Dec 16, 2002
PROLITE / PLASMALITE MPX PULSED LIGHT SYSTEM (PERMANENT HAIR REDUCTION)
General & Plastic Surgery
90d
Cleared
Oct 18, 2002
PLASMALITE PULSED LIGHT SYSTEM
General & Plastic Surgery
88d
Cleared
Aug 29, 2002
PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF UNWANTED HAIR
General & Plastic Surgery
27d
Cleared
Aug 29, 2002
PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS
General & Plastic Surgery
27d
Cleared
Jan 08, 2002
PROLITE PULSED LIGHT SYSTEM FOR THE TREATMENT OF PIGMENTED LESIONS AND THE...
General & Plastic Surgery
90d
Cleared
Jan 08, 2002
PROLITE PULSED LIGHT SYSTEM FOR THE REMOVAL OF UNWANTED HAIR
General & Plastic Surgery
90d
Cleared
Jun 19, 2001
MODIFICATION TO PROLITE PULSED LIGHT SYSTEM
General & Plastic Surgery
83d
Cleared
Jun 19, 2001
PROLITE VL PULSED LIGHT SYSTEM
General & Plastic Surgery
83d
Cleared
Oct 17, 2000
PROLITE PULSED LIGHT SYSTEM
General & Plastic Surgery
209d
Cleared
Sep 11, 2000
PROLITE VL PULSED LIGHT SYSTEM
General & Plastic Surgery
66d