H.P.T. HOME PREG. TEST KIT & A.P.T.— 510(k) K834474
Substantially EquivalentBiomedical Research & Development Laboratories, Inc.
FDA 510(k) clearance K834474 for H.P.T. HOME PREG. TEST KIT & A.P.T., Substantially Equivalent on 1984-09-28. Applicant: Biomedical Research & Development Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Biomedical Research & Development Laboratories, Inc.
- Product code
- Code LCX
- Device class
- Class 2
- Regulation
- 21 CFR 862.1155
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code LCX
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- K243573 — FaStep Early Pregnancy Rapid Test Strip +2 more
More clearances from Biomedical Research & Development Laboratories, Inc.
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