510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K093322Substantially Equivalent

Multi-Purpose Health Device

Upc Medical Supplies, Inc. dba United Pacific Co., San Gabriel CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K093322 is the FDA 510(k) clearance record for MULTI-PURPOSE HEALTH DEVICE, cleared for Upc Medical Supplies, Inc. Dba United Pacific Co. on under FDA product code BWK (Stimulator, Electro-Acupuncture). FDA records list one 510(k) clearance for Upc Medical Supplies, Inc. Dba United Pacific Co. As of , FDA records show no recalls naming K093322.

Clearance record

Decision date
Received
(286 days to decision)
Product code
BWK Stimulator, Electro-Acupuncture
Device class
Unclassified
Review panel
Unknown
Applicant
Upc Medical Supplies, Inc. Dba United Pacific Co. 317 S. San Marino Ave., San Gabriel CA
510(k) summary
Statement
Third party review
No

Clearances, product code BWK

Trailing 12 months

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

FDA records show no clearances under product code BWK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BWK, 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