← FDA Medical Device Classifications
Container, Specimen Mailer And Storage, Temperature Controlled, Sterile
KDW · Class I — Low Risk (general controls) · Pathology · 21 CFR 864.3250
Classification
- FDA Product Code
KDW- Device class
- Class I — Low Risk (general controls)
- Regulation
- 21 CFR 864.3250
- Review panel
- PA
- Medical specialty
- Pathology
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 4
- Registered establishments
- 18
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown