FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DERMAPOINTS MODEL 200 THERAPEUTIC MASSAGER

K Number: K881081 · Decision Jul 21, 1988
Classifications
1
FEI Numbers
176
Registration Numbers
176
Same Product Code
12
Applicant Total
57
Review Days
129

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DERMAPOINTS MODEL 200 THERAPEUTIC MASSAGER
K Number
K881081
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5660
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Ferguson Medical
Date Received
March 14, 1988
Decision Date
July 21, 1988
Product Code
LYG
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
LYG Massager, Therapeutic, Manual

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LYG), ordered by most recent decision date.

View all

Other Clearances by Ferguson Medical

K Number Device Name
K033153 DICOM THEATER
K963794 PUNCTURENEEDLE
K962615 TUMORLOCALIZER MRI
K971813 EMBLA
K972217 ORTHOPEDIC SCREW SYSTEM
K972219 ORTHOPEDIC PLATE SYSTEM
K970819 TARGOBEAM
K970280 FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHESIS OF PER-TROCHANTEROAM FRACTURES
K970258 FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHSIS OF UNSTABLE FEMORAL NECK FRACTURES
K970257 FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHESIS OF SUB-TROCHANTERIAN FRACTURES
Search all 57 clearances from Ferguson Medical →