Miscellaneous devices · 21 CFR 872 Subpart G
Boiling Water Sterilizer
FDA device type “Sterilizer, Boiling Water”.
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 70 in five years
- FDA name
- Sterilizer, Boiling Water
510(k) clearances per year, 1976–2026
510(k) clearances
| Decided | 510(k) | Device | Applicant |
|---|---|---|---|
| 17 Nov 1989 | K895164 | EAGLE DS | American Sterilizer Co. |
| 25 Oct 1984 | K843234 | CITOMAT AUTOCLAVES | Lic-Orthion |
| 16 Jun 1981 | K811237 | MAGNETIC RETENTION UNIT | Universiti Malaya |
| 13 May 1981 | K810977 | ENDODONTIC POST SYSTEMS | Young Innovations Inc |
| 10 Apr 1979 | K790290 | NEY EQUI-HINGE | Deringer-Ney, Inc. |
| 27 Feb 1979 | K790078 | BAR & RIDER, SCREWS, TUBES | Eurodent, Inc. |
| 2 Aug 1977 | K771266 | STEAM STERILIZER | Amsco Hospital Products Co. |
Official records: FDA product classification for ECG · 21 CFR 872.6710.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026