510(k) K895920
K895920 is an FDA 510(k) premarket notification submitted by Vitaphore Corp. for the device "VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS". The FDA issued a decision of Substantially Equivalent on June 6, 1991. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Vitaphore Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 6, 1991
- Date Received
- October 11, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tape And Bandage, Adhesive
- Device Class
- Class I
- Regulation Number
- 880.5240
- Review Panel
- SU
- Submission Type