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INFLATABLE RETENTION CUFF SPECULUM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941391
510(k) Type
Traditional
Applicant
INNOVATEC MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1994
Days to Decision
212 days
Submission Type
Statement

INFLATABLE RETENTION CUFF SPECULUM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941391
510(k) Type
Traditional
Applicant
INNOVATEC MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1994
Days to Decision
212 days
Submission Type
Statement