FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
Program insite® Powder-Free, Disposable Nitrile Exam Gloves
K Number: K252075
·
Decision Oct 17, 2025
Classifications
1
FEI Numbers
380
Registration Numbers
380
Same Product Code
1171
Applicant Total
1
Review Days
107
Basic Information
- Device Name
- Program insite® Powder-Free, Disposable Nitrile Exam Gloves
- K Number
- K252075
- Device Class
- FDA class 1
- Clearance Type
- Abbreviated
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Program Insite, LLC
- Date Received
- July 2, 2025
- Decision Date
- October 17, 2025
- Product Code
- LZA
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LZA | Polymer Patient Examination Glove | FDA class 1 | General Hospital |
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