510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940117Substantially Equivalent - Subject to Tracking Reg.

Mid-500

Block Medical, Inc., Carlsbad CA / Traditional, Substantially Equivalent - Subject to Tracking Reg.
FDA source (opens on fda.gov)

K940117 is the FDA 510(k) clearance record for MID-500, a class II device, cleared for Block Medical, Inc. on under FDA product code MEB (Pump, Infusion, Elastomeric). FDA records list 12 510(k) clearances for Block Medical, Inc., from to . As of , FDA records show no recalls naming K940117.

Clearance record

Decision date
Received
(151 days to decision)
Product code
MEB Pump, Infusion, Elastomeric
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Block Medical, Inc. 5957 Landau Ct., Carlsbad CA
Third party review
No

Clearances, product code MEB

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