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

SL-100 ND:YAG LASER FOR GYNECOLOGY USE

K Number: K871512 · Decision Jul 8, 1988
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
7
Review Days
445

Basic Information

Device Name
SL-100 ND:YAG LASER FOR GYNECOLOGY USE
K Number
K871512
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
MEDICAL ENERGY, INC.
Date Received
April 20, 1987
Decision Date
July 8, 1988
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEX Powered Laser Surgical Instrument

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Other Clearances by MEDICAL ENERGY, INC.

K Number Device Name
K041419 LIGHTFORCE LF 20/30 980NM SURGICAL DIODE LASER SYSTEM
K871511 SL-100 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS
K871514 SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID
K871516 SL-100 ND:YAG LASER FOR UROLOGIC SURGERY
K871515 SL-100 ND:YAG LASER FOR GASTROINTESTINAL BLEEDING
K871513 SL-100 ND:YAG LASER FOR PALLIATION OF GASTRO. MALI