FIRST AID KIT— 510(k) K921976
UnknownThe Home Emergency Room
FDA 510(k) clearance K921976 for FIRST AID KIT, Unknown on 1992-09-10. Applicant: The Home Emergency Room. Device class: 1.
Clearance details
- Applicant
- The Home Emergency Room
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Poway, CA, US
Recent devices under product code LYY
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- K230573 — Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 50 ug per dm2 of glove or less of Total Water Extractable Protein)
- K223298 — Sterile Latex Examination Gloves Powder Free (S, M, L, Extra L)
- K222612 — Powder-Free Latex examination gloves
Data sourced from openFDA. This site is unofficial and independent of the FDA.