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SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921930
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1993
Days to Decision
378 days
Submission Type
Statement

SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921930
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1993
Days to Decision
378 days
Submission Type
Statement