FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

Collagentex Rx-6

K Number: K180585 · Decision May 11, 2018
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
53
Applicant Total
3
Review Days
67

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
Collagentex Rx-6
K Number
K180585
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tanses Technologies, Inc.
Date Received
March 5, 2018
Decision Date
May 11, 2018
Product Code
NHN
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
NHN Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy

Similar 510(k) Clearances

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

View all

Other Clearances by Tanses Technologies, Inc.

K Number Device Name
K162022 Collagentex Rx-1
K152412 T-32;T-40;T-44;T-52;T-72;TT-50