Last synced on 17 May 2024 at 11:06 pm

Electronic Stimulator (Models: uLumb-9530A, uLumb-9531A, uLumb-9532A, uLumb-9533A, LQ-9525B, uNeck-9512A, uNeck-9515A, uNeck-9517B, uNeck-9518A, uNeck-9519A, uNeck-9521A, uNeck-9529A, LQ-9535A)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223428
510(k) Type
Traditional
Applicant
Shenzhen Leqing Medical Instrument Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/8/2023
Days to Decision
175 days
Submission Type
Summary

Electronic Stimulator (Models: uLumb-9530A, uLumb-9531A, uLumb-9532A, uLumb-9533A, LQ-9525B, uNeck-9512A, uNeck-9515A, uNeck-9517B, uNeck-9518A, uNeck-9519A, uNeck-9521A, uNeck-9529A, LQ-9535A)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223428
510(k) Type
Traditional
Applicant
Shenzhen Leqing Medical Instrument Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/8/2023
Days to Decision
175 days
Submission Type
Summary