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LUMISCOPE ALTERNATING PRESSURE PAD & PUMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901096
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1990
Days to Decision
167 days

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901096
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1990
Days to Decision
167 days