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ENDOSCOPIC ANTI-FOG KIT, 100-302-00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933520
510(k) Type
Traditional
Applicant
AVAIL-SOUTHWEST DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1993
Days to Decision
35 days
Submission Type
Statement