← FDA Medical Device Classifications
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
KCT · Class II — Moderate Risk (510(k) clearance required) · General Hospital · 21 CFR 880.6850
Classification
- FDA Product Code
KCT- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 880.6850
- Review panel
- HO
- Medical specialty
- General Hospital
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- Y
Market data
- Cleared 510(k) submissions
- 277
- Registered establishments
- 265
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown