Last synced on 24 June 2022 at 11:05 pm

ADULT ANESTHESIA BREATHING CIRCUIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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