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REBOX II (TENS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895183
510(k) Type
Traditional
Applicant
REBOX (UK) LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
161 days

REBOX II (TENS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895183
510(k) Type
Traditional
Applicant
REBOX (UK) LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
161 days