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ADULT ANESTHESIA BREATHING CIRCUIT

Page Type
Cleared 510(K)
510(k) Number
K932707
510(k) Type
Traditional
Applicant
PRECISION MED PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1993
Days to Decision
49 days
Submission Type
Statement

ADULT ANESTHESIA BREATHING CIRCUIT

Page Type
Cleared 510(K)
510(k) Number
K932707
510(k) Type
Traditional
Applicant
PRECISION MED PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1993
Days to Decision
49 days
Submission Type
Statement