Injection Cap

Q: When was Injection Cap cleared by the FDA?

Injection Cap (K940775) received a 510(k) decision of Substantially Equivalent on June 15, 1994, 113 days after the submission was received.

Q: What is the product code of K940775?

The FDA product code is FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5200.

FDA 510(k) K940775 · Medron, Inc.

Substantially Equivalent

510(k) numberK940775

Submission

Device name: Injection Cap
Applicant: Medron, Inc.
Salt Lake City, UT, US
Received: February 22, 1994
Decision date: June 15, 1994
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code: FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device class: Class II (moderate risk)
Regulation: 21 CFR 880.5200
Specialty: General Hospital

Other 510(k)s with product code FOZ

510(k)	Device	Applicant	Decision
K260432	Ruby Intravascular CatheterFOZ · Traditional	Venocare, Inc.	09/02/2026SE
K260165	Unimpregnated Central Venous CatheterFOZ · Traditional	Spectrum Vascular	08/10/2026SE
K261041	ClearSafe Closed SystemFOZ · Traditional	MedSource Labs, LLC	07/10/2026SE
K260539	MedSource QuickSafe Safety IV Catheter; MedSource PurSafe Safety IV CatheterFOZ · Traditional	MedSource Labs, LLC	07/09/2026SE
K253235	Introcan Safety® Deep Access XL IV CatheterFOZ · Traditional	B.Braun Medical, Inc.	05/15/2026SE
K252137	BD Insyte IV CatheterFOZ · Traditional	Becton Dickinson Infusion Therapy Systems, Inc.	04/02/2026SE
K252513	Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm…FOZ · Special	Poly Medicure Limited	04/01/2026SE
K252398	SURFLO Hybria Closed System Safety IV CatheterFOZ · Traditional	Terumo Medical Products (Hangzhou) Co., Ltd.	12/17/2025SE
K252677	Polyshield Safety IV CathetersFOZ · Special	Poly Medicure Limited	11/05/2025SE
K251422	BD Saf-T-Intima Subcutaneous Catheter SystemFOZ · Traditional	Becton Dickinson Infusion Therapy Systems, Inc.	10/08/2025SE

More from Becton Dickinson Infusion Therapy Systems, Inc.

510(k)	Device	Decision
K192283	MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F…DRE · Traditional	05/06/2020SE
K971897	Continuous Arteriovenous Hemofiltration Catheter 10 FR (Cavh)LFK · Traditional	10/21/1997SE

Questions and answers

When was Injection Cap cleared by the FDA?

Injection Cap (K940775) received a 510(k) decision of Substantially Equivalent on June 15, 1994, 113 days after the submission was received.

What is the product code of K940775?

The FDA product code is FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5200.