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ZEFON ADULT ANESTHESIA BREATHING CIRCUIT

Page Type
Cleared 510(K)
510(k) Number
K924889
510(k) Type
Traditional
Applicant
ZEFON MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1993
Days to Decision
172 days
Submission Type
Summary

ZEFON ADULT ANESTHESIA BREATHING CIRCUIT

Page Type
Cleared 510(K)
510(k) Number
K924889
510(k) Type
Traditional
Applicant
ZEFON MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1993
Days to Decision
172 days
Submission Type
Summary