510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K122978Substantially Equivalent

Saniclave 102, Model Rs-Sc-102

Alternative Pioneering Research and Development, Shafer MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122978 is the FDA 510(k) clearance record for SANICLAVE 102, MODEL RS-SC-102, a class II device, cleared for Alternative Pioneering Research and Development on under FDA product code FLE (Sterilizer, Steam). FDA records list 2 510(k) clearances for Alternative Pioneering Research and Development, from to . As of , FDA records show no recalls naming K122978.

Clearance record

Decision date
Received
(239 days to decision)
Product code
FLE Sterilizer, Steam
Regulation
21 CFR 880.6880
Device class
Class II
Review panel
General Hospital
Applicant
Alternative Pioneering Research and Development 17319 Lake Blvd., Shafer MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FLE

Trailing 12 months
4 clearances under product code FLE in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FLE, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20261
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260