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TURKEL PNEUMOTHORAX KIT

Page Type
Cleared 510(K)
510(k) Number
K923028
510(k) Type
Traditional
Applicant
SYMBIOSIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1992
Days to Decision
42 days
Submission Type
Statement

TURKEL PNEUMOTHORAX KIT

Page Type
Cleared 510(K)
510(k) Number
K923028
510(k) Type
Traditional
Applicant
SYMBIOSIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1992
Days to Decision
42 days
Submission Type
Statement