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ZEPHYR 'X-SERIES PATIENT TRANSFER SLED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121929
510(k) Type
Traditional
Applicant
DIACOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2013
Days to Decision
199 days
Submission Type
Summary

ZEPHYR 'X-SERIES PATIENT TRANSFER SLED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121929
510(k) Type
Traditional
Applicant
DIACOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2013
Days to Decision
199 days
Submission Type
Summary