ACU-TEST IN-HOME PREGNANCY TEST— 510(k) K781049
Substantially EquivalentWilliams, the J.B. Co., Inc.
FDA 510(k) clearance K781049 for ACU-TEST IN-HOME PREGNANCY TEST, Substantially Equivalent on 1978-06-29. Applicant: Williams, the J.B. Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Williams, the J.B. Co., Inc.
- Product code
- Code JHJ
- Device class
- Class 2
- Regulation
- 21 CFR 862.1155
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code JHJ
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