K961502Substantially Equivalent
Lubricating Jelly, Low Viscosity
Span-America Medical Systems, Inc., Greenville SC / Traditional, Substantially Equivalent
K961502 is the FDA 510(k) clearance record for LUBRICATING JELLY, LOW VISCOSITY, a class I device, cleared for Span-America Medical Systems, Inc. on under FDA product code KMJ (Lubricant, Patient). FDA records list 19 510(k) clearances for Span-America Medical Systems, Inc., from to . As of , FDA records show no recalls naming K961502.
Clearance record
- Decision date
- Received
- (90 days to decision)
- Product code
- KMJ Lubricant, Patient
- Regulation
- 21 CFR 880.6375
- Device class
- Class I
- Review panel
- General Hospital
- Applicant
- Span-America Medical Systems, Inc. 70 Commerce Dr., Greenville SC
- 510(k) summary
- Summary
- Third party review
- No
Clearances, product code KMJ
Trailing 12 monthsFDA records hold no clearances under product code KMJ in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
