FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

Curapuls 670

K Number: K243112 · Decision Jun 25, 2025
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
44
Applicant Total
5
Review Days
268

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Basic Information

Device Name
Curapuls 670
K Number
K243112
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5290
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Enraf-Nonius, B.V.
Date Received
September 30, 2024
Decision Date
June 25, 2025
Product Code
IMJ
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
IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

Similar 510(k) Clearances

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

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Other Clearances by Enraf-Nonius, B.V.

K Number Device Name
K251083 Compact II
K230472 Sonopuls 190
K151640 ELTRAC 471
K030297 FLEXIBLE RUBBER ELECTRODES, MODELS: 1460265, 1460272, 1460274, 3444128, 3444129, 3444130