510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934434Substantially Equivalent

Cyberrx Model 7200

Cybermed Control Systems, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934434 is the FDA 510(k) clearance record for CYBERRX MODEL 7200, a class I device, cleared for Cybermed Control Systems, Inc. on under FDA product code FFT (Electrode, Ph, Stomach). FDA records list one 510(k) clearance for Cybermed Control Systems, Inc. As of , FDA records show no recalls naming K934434.

Clearance record

Decision date
Received
(519 days to decision)
Product code
FFT Electrode, Ph, Stomach
Regulation
21 CFR 876.1400
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Cybermed Control Systems, Inc. 12770 High Bluff Dr., San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code FFT

Trailing 12 months

FDA records hold no clearances under product code FFT in the trailing twelve months.

FDA records show no clearances under product code FFT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FFT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260