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PM3000 & PM3100 VACUUM REGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922817
510(k) Type
Traditional
Applicant
PRECISION MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1993
Days to Decision
266 days
Submission Type
Statement

PM3000 & PM3100 VACUUM REGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922817
510(k) Type
Traditional
Applicant
PRECISION MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1993
Days to Decision
266 days
Submission Type
Statement