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MEROCEL(R) TURBINATE GLOVE AND SEPTAL SPLINT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935658
510(k) Type
Traditional
Applicant
MEROCEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1994
Days to Decision
100 days
Submission Type
Statement

MEROCEL(R) TURBINATE GLOVE AND SEPTAL SPLINT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935658
510(k) Type
Traditional
Applicant
MEROCEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1994
Days to Decision
100 days
Submission Type
Statement