PHARMASEAL GENETIC AMNIOCENTESIS TRAY— 510(k) K894031
UnknownBaxter Healthcare Corp
FDA 510(k) clearance K894031 for PHARMASEAL GENETIC AMNIOCENTESIS TRAY, Unknown on 1989-08-04. Applicant: Baxter Healthcare Corp. Device class: 1.
Clearance details
- Applicant
- Baxter Healthcare Corp
- Product code
- Code HIO
- Device class
- Class 1
- Regulation
- 21 CFR 884.1550
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Valencia, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.