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EXPANDACELL ANTI-FOG INSTRUMENT WIPE (WITH ALCOHOL)/(WITHOUT)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964334
510(k) Type
Traditional
Applicant
SHIPPERT MEDICAL TECHNOLOGIES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1996
Days to Decision
39 days
Submission Type
Summary

EXPANDACELL ANTI-FOG INSTRUMENT WIPE (WITH ALCOHOL)/(WITHOUT)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964334
510(k) Type
Traditional
Applicant
SHIPPERT MEDICAL TECHNOLOGIES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1996
Days to Decision
39 days
Submission Type
Summary