510(k) K912367
K912367 is an FDA 510(k) premarket notification submitted by Aaron Medical Industries for the device "EYE BUBBLE". The FDA issued a decision of Substantially Equivalent on October 2, 1991. The device falls under product code HOY (Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)), a Class I device regulated under 21 CFR 886.4750. Aaron Medical Industries has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 2, 1991
- Date Received
- May 29, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- Device Class
- Class I
- Regulation Number
- 886.4750
- Review Panel
- OP
- Submission Type