510(k) K780033
- Device
- MATTRESSES, CONDUCTIVE & COVERS
- Applicant
- CHASE MFG. CO.
- 510(k) number
- K780033
- Product code
- FMW
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-02-21
- Date received
- 1978-01-09
- Regulation
- 880.6190
- Classification name
- Cover, Mattress (medical Purposes)
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3034728569
- 3038623066
- 3014345255
- 3017070378
- 3007212927
- 1836161
- 3033506545
- 3014674312
- 3011556876
- 3010580775
- 3002637602
- 3007798904
- 3011621895
- 1649595
- 3015526463
- 3012316249
- 3004475699
- 3008518417
- 3014928153
- 3008541934
- 3012392312
- 3012775375
- 3018084435
- 3037012186
- 2428983
- 3017171460
- 3008392711
- 9615245
- 8022890
- 3033883981
- 3038718579
- 3010595915
- 3009273990
- 3014739961
- 3006803543
- 1043644
- 3005864972
- 8022611
- 1527185
- 3031980467
- 3038285060
- 1523547
- 3045009498
- 3009008046
- 3007008421
- 3010625818
- 3004158259
- 3017171467
- 3023339277
- 3015219076
- 3016457665
- 3044819802
- 3010383831
- 3015337373
- 3016712364
- 3016914692
- 3013684902
- 3011497662
- 1933975
- 3013298431
- 3010890274
- 3008630266
- 1065597
- 3008410069
- 3015288041
- 1932271
- 1528695
- 3015068387
- 3006537699
- 3029983606
- 2032476
- 3005179379
- 3013685983
- 3031027
- 3030078769
- 8030877
- 3008427684
- 1000133289
- 3017953189
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FMW #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K152884 | DermaTherapy Bed Linens | Precision Fabrics Group, Inc. | 2016-06-20 |
| K061242 | DERMATHERAPY, MODEL 22216 | Precision Fabrics Group, Inc. | 2007-01-25 |
| K001003 | Z-NET | Demite Limited | 2001-12-10 |
| K992702 | EVENT ALLERGEN BARRIERS, EVENT MATTRESS ENCASING, EVENT DUVET ENCASING, EVENT PILLOW ENCASING, EVENT BEDDING SYSTEM | Allergy Direct | 1999-11-08 |
| K940327 | INTERVENT ALLERGEN EXCLUSION TECHNOLOGY, INTERVENT BEDDING SYSTEM, INTERVENT MATTRESS INTERLINER, INTERVIEW PILLOW | W. L. Gore & Associates, Inc. | 1994-02-25 |
| K935220 | CORE PREVENT MATTRESS MODIFICATION | Paladin Medical, Inc. | 1993-11-29 |
| K924807 | REUSABLE INCONTIENT UNDERPAD | Perfect Fit Industries, Inc. | 1993-02-10 |
| K924477 | WIPEABLE PILLOW | Perfect Fit Industries, Inc. | 1993-01-29 |
| K921928 | SOFT-COVER | Adroit Medical Systems, Inc. | 1992-11-06 |
| K923173 | OBALON COVER | Turnsoft, Inc. | 1992-11-06 |
| K903382 | ALLERGY CONTROL COVERS | Allergy Control Products, Inc. | 1990-11-02 |
| K902446 | DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST | Mallinckrodt Group, Inc. | 1990-08-10 |
| K832483 | MATTRESS COVER, ANTI-MICROBIAL | American Threshold Industries, Inc. | 1984-02-04 |
Legacy Summary#
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FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases