PRE-ROLLED TUBULAR STOCKINETTE
FDA 510(k) clearance K831936 · decided 1983-12-30
Clearance details
- K-number
- K831936
- Device name
- PRE-ROLLED TUBULAR STOCKINETTE
- Applicant
- Ormed Mfg., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1983-06-15
- Decision date
- 1983-12-30
- Days to decision
- 198 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.