FDA 510(k) Substantially Equivalent 🇺🇸 United States

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY

K Number: K827506 · Decision Jun 11, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
6
Review Days
38

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Basic Information

Device Name
MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY
K Number
K827506
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Merrimack Laboratories
Date Received
May 4, 1982
Decision Date
June 11, 1982
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

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