← FDA Medical Device Classifications
Magnet, Test, Pacemaker
DTG · Class I — Low Risk (general controls) · Cardiovascular · 21 CFR 870.3690
Classification
- FDA Product Code
DTG- Device class
- Class I — Low Risk (general controls)
- Regulation
- 21 CFR 870.3690
- Review panel
- CV
- Medical specialty
- Cardiovascular
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 5
- Registered establishments
- 6
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown