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PRECISION MED PRODUCTS, LTD. ADULT GAS SAMPLING

Page Type
Cleared 510(K)
510(k) Number
K932497
510(k) Type
Traditional
Applicant
PRECISION MED PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
59 days
Submission Type
Statement

PRECISION MED PRODUCTS, LTD. ADULT GAS SAMPLING

Page Type
Cleared 510(K)
510(k) Number
K932497
510(k) Type
Traditional
Applicant
PRECISION MED PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
59 days
Submission Type
Statement