510(k) K953241
- Device
- EXSPOR
- Applicant
- ALCIDE CORP.
- 510(k) number
- K953241
- Product code
- LKX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1995-09-29
- Date received
- 1995-07-11
- Regulation
- 510(k) Premarket Notification
- Classification name
- Device, Thermal, Hemorrhoids
- Medical specialty
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Review panel
- Gastroenterology/Urology
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- No
Applicant Contact#
- Contact
- JOHN P RICHARDS
- Address
- 8561 154th Ave., NE Redmond WA US 98052 98052
FDA Registration Numbers#
- 3013735158
- 3012119286
- 3003074886
- 3030017177
- 1055757
- 3042277215
- 2183301
- 1926681
- 3008250583
- 3013526605
- 3006517436
- 3044466317
- 3016758972
- 3016457665
- 3030040496
- 2121746
- 3011689956
- 3013521223
- 3016860525
- 3007573469
- 3012187973
- 3014437893
- 3013547614
- 3016671078
- 3016712306
- 3029507159
- 3008951115
- 1422443
- 3010374972
- 3010700223
- 3042261316
- 3007420701
- 3009233038
- 3004080548
- 8040277
- 2225311
- 3008496560
- 3005798905
- 3007517215
- 3015422337
- 3008973760
- 1722021
- 8022656
- 3013865802
- 3016872092
- 3038285060
- 3017178443
- 3004496839
- 3017125427
- 3034669683
- 1423537
- 3005533873
- 2024980
- 3008427684
- 3008808082
- 3006210673
- 3011310668
- 3000246414
- 3023341288
- 3024988170
- 3016816754
- 8040278
- 3008697511
- 1063707
- 3034733579
- 3028013069
- 3008770252
- 3016171962
- 3008763803
- 3017674087
- 2129284
- 3011182134
- 1932672
- 3007050292
- 1319130
- 3023176408
- 3004617746
- 3025440611
- 3005078659
- 3030896267
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code LKX #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K172358 | Instalief | Privi Medical Pte, Ltd. | 2018-01-10 |
| K113660 | COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICAL | Cryotherapy Products, Inc. | 2012-05-03 |
| K072414 | CRYOSTAT | Lil Drug Store Products, Inc. | 2008-04-07 |
| K042564 | HEMOR-RITE CRYOTHERAPHY | Fama Holdings International Corp | 2005-09-30 |
| K012746 | ICE BATON | Behive, Ltd. | 2001-11-14 |
| K981428 | ANU ICE | Cryoptherapy Pain Relief Products, Inc. | 1998-07-07 |
| K973590 | HEMORRELIEF DEVICE | A.Stein - Regulatory Affairs Consulting | 1998-02-05 |
| K944874 | ZEROID HEMORRHOIDAL DEVICE | Medical Appliance Research Corp. | 1995-08-07 |
| K921189 | THERMA-H | Zewa AG | 1992-08-31 |
| K905276 | THERMA-H | Kure Swiss Medical AG Corp. | 1991-11-07 |
| K883984 | HEMORX COLD PACK | Bio-Dyne, Inc. | 1988-12-22 |
| K862490 | ANU-RX | J. & Jp., Inc. | 1986-08-18 |
| K855150 | HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS | Hpk International, Inc. | 1986-04-01 |
| K854569 | HEMOR-ICE | Technology 2000 | 1986-02-05 |
| K852679 | MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICE | J. & Jp., Inc. | 1985-08-09 |
Legacy Summary#
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
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