Isolation Masks
FDA 510(k) K893939 · James River Corp.
510(k) numberK893939
Submission
- Device name
- Isolation Masks
- Applicant
- James River Corp.
Neenah, WI, US - Received
- May 31, 1989
- Decision date
- July 14, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FXX – Mask, Surgical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4040
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code FXX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K251967 | HALYARD* FLUIDSHIELD* 3 Fog-Free Procedure Mask with SO SOFT* Lining and SO SOFT*…FXX · Traditional | O&M Halyard, Inc. | 03/18/2026SE |
| K252534 | Surgical Face Mask (Ear mount)FXX · Traditional | Zhejiang Hangkang Medical Equipment Co., Ltd. | 03/03/2026SE |
| K253398 | Disposable Surgical Mask (Non-Sterile) (EFX3PLBLKMSK300)FXX · Special | Efofex, Inc. | 02/19/2026SE |
| K252830 | Disposable Surgical Face Mask (3P00B, C2900)FXX · Traditional | Beatles Medical Supplies (Xiantao) Co., Ltd. | 01/12/2026SE |
| K252650 | Disposable Medical Face MaskFXX · Traditional | Makrite Industries, Inc. | 01/05/2026SE |
| K243342 | KP Protective Face MaskFXX · Traditional | Kp Trading Co., Ltd. | 12/22/2025SE |
| K252941 | HALYARD* Adult Face Mask with SO SOFT* Lining and SO SOFT* EarloopsFXX · Traditional | O&M Halyard, Inc. | 12/11/2025SE |
| K252964 | PRIMED Surgical and Procedure MasksFXX · Traditional | Primed Medical Products, Inc. | 11/04/2025SE |
| K251902 | Vitaform Procedural Mask - Blue (Vitaform Blue); Vitaform Procedural Mask with Shield…FXX · Traditional | Vitacore Industries, Inc. | 09/17/2025SE |
| K250082 | Procedure mask/Surgical mask/Face maskFXX · Traditional | Winner Medical Co., Ltd. | 06/18/2025SE |
More from Winner Medical Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K894505 | Cotolin Drain Sponge and Dressing SpongeEFQ · Traditional | 09/15/1989SE |
| K894147 | Visulin Transparent Adhesive DressingKGX · Traditional | 08/09/1989SN |
| K894034 | Modified Labeling of Surgical GlovesKGO · Traditional | 07/14/1989SE |
| K892580 | Caretouch Examination GlovesLYY · Traditional | 07/14/1989SE |
| K890459 | James River Biogel Powderless Surgical GlovesKGO · Traditional | 04/20/1989SE |
| K883802 | Caretex Central Supply WrapFRG · Traditional | 10/21/1988SE |
| K884112 | Caretex or TowelKKX · Traditional | 10/13/1988SE |
| K883657 | Skid Resistant, Long Lasting Shoe CoversFXP · Traditional | 09/15/1988SE |
| K880481 | Caretex Surgeon's CapsFYF · Traditional | 02/24/1988SE |
| K880431 | Caretex Surgeon's HoodsFXY · Traditional | 02/24/1988SE |
Questions and answers
When was Isolation Masks cleared by the FDA?
Isolation Masks (K893939) received a 510(k) decision of Substantially Equivalent on July 14, 1989, 44 days after the submission was received.
What is the product code of K893939?
The FDA product code is FXX – Mask, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.