Clearance Summary
PROBE(TM) MODELS 700 AND 1000 received FDA 510(k) clearance under submission number K883749, sponsored by Packard Instrument Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1988-11-10.
- Submission: K883749
- Applicant / Sponsor: Packard Instrument Co., Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2750
- Decision date: 1988-11-10
Classification & Regulation
This clearance is catalogued under FDA product code JQW and 21 CFR 862.2750, within the Clinical Chemistry review panel as a Class I device.