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MERETEK BREATH TEST FOR H.PYLORI COLLECTION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952220
510(k) Type
Traditional
Applicant
MERETEK DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1996
Days to Decision
495 days
Submission Type
Statement

MERETEK BREATH TEST FOR H.PYLORI COLLECTION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952220
510(k) Type
Traditional
Applicant
MERETEK DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1996
Days to Decision
495 days
Submission Type
Statement