ENTERO-TEST HP, MODEL #102-01— 510(k) K983119
Substantially EquivalentHdc Corp.
FDA 510(k) clearance K983119 for ENTERO-TEST HP, MODEL #102-01, Substantially Equivalent on 1999-03-15. Applicant: Hdc Corp.. Device class: 1.
Clearance details
- Applicant
- Hdc Corp.
- Product code
- Code LIO
- Device class
- Class 1
- Regulation
- 21 CFR 866.2900
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.