510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K970857Substantially Equivalent

Argyle Aqua-Seal All Purpose Autotransfusion Chest Drainage Unit and Optional Argyle Aqua-Seal Evacuating Autotransfusio

Davis & Geck, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970857 is the FDA 510(k) clearance record for ARGYLE AQUA-SEAL ALL PURPOSE AUTOTRANSFUSION CHEST DRAINAGE UNIT AND OPTIONAL ARGYLE AQUA-SEAL EVACUATING AUTOTRANSFUSIO, a class II device, cleared for Davis & Geck, Inc. on under FDA product code CAC (Apparatus, Autotransfusion). FDA records list 45 510(k) clearances for Davis & Geck, Inc., from to . As of , FDA records show no recalls naming K970857.

Clearance record

Decision date
Received
(240 days to decision)
Product code
CAC Apparatus, Autotransfusion
Regulation
21 CFR 868.5830
Device class
Class II
Review panel
Anesthesiology
Applicant
Davis & Geck, Inc. 1915 Olive St., St. Louis MO
510(k) summary
Summary
Third party review
No

Clearances, product code CAC

Trailing 12 months

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

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