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#
- 3017417635
- 3010175283
- 3010131137
- 3012709011
- 3045742729
- 2086043
- 3014819517
- 3013865802
- 3015937050
- 9612030
- 3011248163
- 3015277818
- 3003965504
- 3012119286
- 3038276119
- 3013684902
- 3007420701
- 3004496839
- 3004604967
- 3017140435
- 3007649424
- 1422443
- 3043153468
- 3014420447
- 3012466144
- 3016756928
- 3006416350
- 3042261316
- 3014276660
- 3005327291
- 3043748032
- 3017199830
- 3030534974
- 3007573469
- 3017236126
- 3030040496
- 3037314258
- 2024980
- 3007770329
- 3011508621
- 3014739961
- 3045058049
- 3016872092
- 3029507159
- 3016195105
- 3014368824
- 3005460813
- 3024082778
- 3014437893
- 3008763803
- 3009609749
- 3025440611
- 3017293064
- 3015821396
- 3008114965
- 3016965811
- 3005798905
- 3003965134
- 3019315696
- 3011689956
- 3038285060
- 3013526605
- 3008264242
- 3005380088
- 3007120504
- 3018507299
- 3004857344
- 3023176408
- 3006851654
- 3016457675
- 3011434305
- 3011611571
- 1219113
- 3011310668
- 1815703
- 3006550126
- 3016447764
- 2087075
- 3014626425
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