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#
- 3042277215
- 3003520997
- 3045058049
- 3008912871
- 3029507159
- 3016756928
- 3018507299
- 3015937050
- 3007748817
- 3011182134
- 3003887292
- 3004176176
- 3014883395
- 3013123550
- 3003890648
- 3008114965
- 9710020
- 3009609749
- 3016758972
- 3015140351
- 3043153496
- 3010380285
- 3033920063
- 2435946
- 3015084765
- 3012119286
- 3017618900
- 3011360380
- 3005798905
- 3016450032
- 3010683450
- 3014739961
- 3042989733
- 3007649424
- 3013525704
- 3011689956
- 2029076
- 3030019992
- 3015378469
- 3026858378
- 3008264242
- 3005327291
- 8040172
- 3004014222
- 3014631422
- 3019356454
- 3014146451
- 3021635975
- 3014819517
- 3006851654
- 3012314549
- 9680413
- 3015729
- 3014426541
- 1932672
- 3038276119
- 1063707
- 3010402957
- 3009540516
- 3005083505
- 3039396083
- 1937310
- 3024988170
- 2022388
- 3016447764
- 3030856996
- 2129284
- 2087075
- 3008494300
- 1423537
- 3039322966
- 3004993527
- 3030896267
- 3007420701
- 3008044603
- 3027605322
- 3039435282
- 9616872
- 3032109
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