510(k) K922177
K922177 is an FDA 510(k) premarket notification submitted by Allergy Extract Co. for the device "DISPOSABLE MULTI-PUNCTURE APPLICATOR". The FDA issued a decision of Substantially Equivalent on June 17, 1993. The device falls under product code SCL (Allergen And Vaccine Delivery Needles), a Class II device regulated under 21 CFR 880.5570.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 17, 1993
- Date Received
- May 8, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Allergen And Vaccine Delivery Needles
- Device Class
- Class II
- Regulation Number
- 880.5570
- Review Panel
- HO
- Submission Type
An allergen delivery needle is a device intended to percutaneously deliver diagnostic allergenic extracts for use in allergy skin tests also referred to as skin prick tests or intradermal allergy tests.