510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930313Substantially Equivalent

Apex Specimen Bag

Apex Medical Technologies, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930313 is the FDA 510(k) clearance record for APEX SPECIMEN BAG, a class I device, cleared for Apex Medical Technologies, Inc. on under FDA product code LIO (Device, Specimen Collection). FDA records list 8 510(k) clearances for Apex Medical Technologies, Inc., from to . As of , FDA records show no recalls naming K930313.

Clearance record

Decision date
Received
(55 days to decision)
Product code
LIO Device, Specimen Collection
Regulation
21 CFR 866.2900
Device class
Class I
Review panel
Microbiology
Applicant
Apex Medical Technologies, Inc. 10064 Mesa Ridge Ct., #202, San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code LIO

Trailing 12 months

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

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