Last synced on 16 May 2025 at 11:05 pm

HEMDETECT(R) TEST FOR OCCULT BLOOD IN FECES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936056
510(k) Type
Traditional
Applicant
DIPRO DIAGNOSTIC PRODUCTS GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1995
Days to Decision
471 days
Submission Type
Statement

HEMDETECT(R) TEST FOR OCCULT BLOOD IN FECES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936056
510(k) Type
Traditional
Applicant
DIPRO DIAGNOSTIC PRODUCTS GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1995
Days to Decision
471 days
Submission Type
Statement