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PATIENT RESTRAINT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K771659
510(k) Type
Traditional
Applicant
MTD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1977
Days to Decision
31 days

PATIENT RESTRAINT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K771659
510(k) Type
Traditional
Applicant
MTD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1977
Days to Decision
31 days