Clearance Summary
PINLOCK CONTAINER received FDA 510(k) clearance under submission number K770071, sponsored by Perkins Mfg. Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1977-02-24.
- Submission: K770071
- Applicant / Sponsor: Perkins Mfg. Co.
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class I
- Regulation citation: 21 CFR 864.3250
- Decision date: 1977-02-24
Classification & Regulation
This clearance is catalogued under FDA product code KDT and 21 CFR 864.3250, within the Pathology review panel as a Class I device.