Parexel Intl. Corp.
Parexel Intl. Corp. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 9, 1991.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K900385 | ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGE | July 9, 1991 |
| K904902 | SMA 26 TRANSDUCER | March 26, 1991 |
| K904901 | L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC | March 26, 1991 |
| K884800 | ACTA GENOS ELECTROCARDIOGRAPH | June 22, 1989 |
| K862414 | FUJI CR IMAGING PLATE | February 26, 1987 |
| K864519 | PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR) | February 13, 1987 |
| K862416 | FTI 100 MEDICAL THERMAL IMAGER | July 1, 1986 |
| K862415 | TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM | July 1, 1986 |
| K853295 | EMODREN EXCHANGEABLE PLASTIC BELLOWS | August 20, 1985 |
| K853296 | EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODREN | August 15, 1985 |
| K851322 | PERSONAL C3 3-CHANNEL ELECTROCARDIOGRAPH | May 16, 1985 |
| K842123 | PERSONAL CL SINGLE-CHANNEL ELECTROCAR | November 16, 1984 |
| K842208 | NATURA-TONE OR LUXOPAL CL ACRYLIC | July 31, 1984 |
| K841826 | NATURA-DENT VACUUM-FIRED PORCELAIN TEETH | July 12, 1984 |