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STEAM STERILIZER, 3000

K770536 Class II Traditional
Decision Date
1977-04-29
Sponsor / Applicant
Castle Co.

Technical Specification

510(k) Submission ID K770536
Product Code FLE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6880
Decision Date 1977-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STEAM STERILIZER, 3000 received FDA 510(k) clearance under submission number K770536, sponsored by Castle Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1977-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code FLE and 21 CFR 880.6880, within the General Hospital review panel as a Class II device.