Cavity Drainage Catheterization Set, CS-01600

FDA 510(k) K895516 · Arrow Intl., Inc.

Substantially Equivalent

510(k) numberK895516

Submission

Device name
Cavity Drainage Catheterization Set, CS-01600
Applicant
Arrow Intl., Inc.
Reading, PA, US
Received
September 12, 1989
Decision date
December 27, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GBX – Catheter, Irrigation
Device class
Class I (low risk)
Regulation
21 CFR 878.4200
Specialty
General, Plastic Surgery

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Questions and answers

When was Cavity Drainage Catheterization Set, CS-01600 cleared by the FDA?

Cavity Drainage Catheterization Set, CS-01600 (K895516) received a 510(k) decision of Substantially Equivalent on December 27, 1989, 106 days after the submission was received.

What is the product code of K895516?

The FDA product code is GBX – Catheter, Irrigation, a Class I (low risk) device regulated under 21 CFR 878.4200.