510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K973693Substantially Equivalent for Some Indications

Aqua Patch

Pci Technology, Dallas TX / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K973693 is the FDA 510(k) clearance record for AQUA PATCH, cleared for Pci Technology on under FDA product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic). FDA records list one 510(k) clearance for Pci Technology. As of , FDA records show no recalls naming K973693.

Clearance record

Decision date
Received
(83 days to decision)
Product code
MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Device class
Unclassified
Review panel
Unknown
Applicant
Pci Technology 10969 Shady Trl., Dallas TX
Third party review
No

Clearances, product code MGQ

Trailing 12 months

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

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