ECGClass I
Sterilizer, Boiling Water
21 CFR 872.6710 / Dental
ECG is the FDA product code for Sterilizer, Boiling Water, a class I device type, regulated under 21 CFR 872.6710. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- ECG
- Device name
- Sterilizer, Boiling Water
- Regulation
- 21 CFR 872.6710
- Device class
- Class I
- Review panel
- Dental
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 7
- Ingested recalls
- 0
Clearances, product code ECG
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 1 |
| 1979 | 2 |
| 1981 | 2 |
| 1984 | 1 |
| 1989 | 1 |
Applicants with the most clearances
Product code ECG| Applicant | Clearances |
|---|---|
| American Sterilizer Co. | 1 |
| Amsco Hospital Products Co. | 1 |
| Deringer-Ney, Inc. | 1 |
| Eurodent, Inc. | 1 |
| Lic-Orthion | 1 |
| Preat Corp. | 1 |
| Universiti Malaya | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeNo registered establishment in MDM’s records lists product code ECG.
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