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MODEL 561 C-ARM PROCEDURES STRETCHER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923730
510(k) Type
Traditional
Applicant
MIDMARK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1994
Days to Decision
562 days
Submission Type
Statement

MODEL 561 C-ARM PROCEDURES STRETCHER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923730
510(k) Type
Traditional
Applicant
MIDMARK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1994
Days to Decision
562 days
Submission Type
Statement