510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K972122Substantially Equivalent

Dream Catcher

Rest Technologies, Inc., Santa Monica CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972122 is the FDA 510(k) clearance record for DREAM CATCHER, a class II device, cleared for Rest Technologies, Inc. on under FDA product code GXY (Electrode, Cutaneous). FDA records list one 510(k) clearance for Rest Technologies, Inc. As of , FDA records show no recalls naming K972122.

Clearance record

Decision date
Received
(85 days to decision)
Product code
GXY Electrode, Cutaneous
Regulation
21 CFR 882.1320
Device class
Class II
Review panel
Neurology
Applicant
Rest Technologies, Inc. 827 20th St., Santa Monica CA
510(k) summary
Statement
Third party review
No

Clearances, product code GXY

Trailing 12 months
11 clearances under product code GXY in the twelve months to October 2026, May 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code GXY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20261
April 20262
May 20263
June 20262
July 20261
August 20261
September 20260
October 20260