Last synced on 14 November 2025 at 11:06 pm

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

Page Type
Cleared 510(K)
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)
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