Last synced on 12 August 2022 at 11:05 pm

STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC19100, SPC19150, SPC18050,SPC18100,SPC18150

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082772
510(k) Type
Traditional
Applicant
LIFE-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2009
Days to Decision
140 days
Submission Type
Statement

STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC19100, SPC19150, SPC18050,SPC18100,SPC18150

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082772
510(k) Type
Traditional
Applicant
LIFE-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2009
Days to Decision
140 days
Submission Type
Statement