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#
- 2225311
- 3021635975
- 3011611571
- 3016671078
- 3016458366
- 3008352964
- 3017248120
- 1526481
- 3004753270
- 3015378469
- 3030528528
- 3007748817
- 3014314985
- 1937310
- 3011310668
- 3013524663
- 3017125427
- 3007050292
- 3017618900
- 3025413691
- 3017889736
- 2024980
- 3015139713
- 3017654286
- 3012709011
- 1450386
- 3009666019
- 3039396083
- 3032109
- 3015168743
- 3008808082
- 3009848807
- 3008808560
- 1922337
- 9613418
- 3007420694
- 3012119286
- 3016171962
- 3009233038
- 2121746
- 3039322966
- 3015142802
- 3002714597
- 3011360380
- 3042277215
- 3014437893
- 9680413
- 1815703
- 8040172
- 3027645317
- 3003965504
- 3007649424
- 1932672
- 3013518061
- 3006517436
- 3005533873
- 3027529712
- 3035732161
- 3008763803
- 3019315696
- 3017199830
- 3017293064
- 3005951243
- 3009540516
- 3013427445
- 3010602043
- 3010374972
- 3003887292
- 3047528398
- 3008044603
- 3014108257
- 3009148458
- 1721183
- 3043126908
- 3014883395
- 3016510805
- 3006851654
- 3015363935
- 3003927385
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#
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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