NITRILE PATIENT EXAMINATION GLOVES, POWDERED, NON-STERILE
FDA 510(k) clearance K992558 · decided 1999-09-27
Clearance details
- K-number
- K992558
- Device name
- NITRILE PATIENT EXAMINATION GLOVES, POWDERED, NON-STERILE
- Applicant
- Riverstone Resources Sdn Bhd
- Decision
- Substantially Equivalent
- Date received
- 1999-07-30
- Decision date
- 1999-09-27
- Days to decision
- 59 days
- Clearance type
- Traditional
- Product code
- LZA
- Device class
- 1
- Regulation number
- 880.6250
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Kepong Baru, Kuala Lumpur, MY
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Riverstone Resources Sdn Bhd
The Builder collects up to 8 candidate devices side by side with yours, then exports the substantial-equivalence comparison scaffold. How it works
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.