510(k) K840835
- Device
- STRAITH DRAIN INSERTER
- Applicant
- SURGICAL TECHNOLOGY LABORATORIES, INC.
- 510(k) number
- K840835
- Product code
- FZX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-04-23
- Date received
- 1984-02-24
- Regulation
- 878.4800
- Classification name
- Guide, Surgical, Instrument
- Medical specialty
- General & Plastic Surgery
- Review panel
- General & Plastic Surgery
- 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#
- 2031009
- 3012434811
- 3009051471
- 3008720584
- 3010197239
- 1054986
- 3042235752
- 1526534
- 1315756
- 3003694247
- 8044098
- 3005809810
- 3005641619
- 2183449
- 9611390
- 3002719998
- 3004837686
- 3015877656
- 9611112
- 3008114965
- 3010388970
- 3010160527
- 1055890
- 3005751028
- 1038671
- 3009513193
- 1054811
- 2184009
- 3003435550
- 9680825
- 9617297
- 3009468807
- 3021010222
- 9610622
- 1721504
- 9611610
- 3011301313
- 3038503932
- 3013011598
- 3023155873
- 3009582259
- 1018233
- 3010303097
- 9680735
- 3007200016
- 1828288
- 9613350
- 8010343
- 3029082594
- 3014207283
- 3002907620
- 1064017
- 3010123206
- 3009882462
- 3007366790
- 3014662844
- 1045834
- 3011365613
- 3023852420
- 3038187464
- 8031020
- 3032391
- 1030489
- 3009971621
- 3019356409
- 3017565094
- 3009173317
- 3014302784
- 3011061242
- 3007319107
- 3008771447
- 9615765
- 3012494290
- 3009887475
- 3006563559
- 9611461
- 3027071765
- 3009590742
- 3009631939
- 3003322138
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FZX #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K914715 | PARALLELING GUIDES | Implant Corp. of America | 1994-02-16 |
| K871413 | CIVCO STEPPER | CIVCO Medical Instruments Co., Inc. | 1987-07-14 |
| K871503 | BIOPSY NEEDLE GUIDE KIT, STERILE | Amedic USA | 1987-07-10 |
| K862564 | A.C.L. GUIDE KIT | Aspen Laboratories, Inc. | 1986-08-18 |
| K854262 | MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY | Meadox Surgimed, Inc. | 1985-12-24 |
| K852402 | NAMIC HOMER MAMMALOK NEEDLE/WIRE LOCALIZER | North American Instrument Corp. | 1985-07-11 |
| K842698 | BRITISH SPINAL FUSION SET | Downs Surgical , Ltd. | 1984-09-12 |
| K841618 | THREADING TUBE | Plastafil, Inc. | 1984-08-27 |
| K841619 | DRILL GUIDE | Plastafil, Inc. | 1984-07-11 |
| K841297 | TECHMEDICA DRILL GUIDE | Techmedica, Inc. | 1984-04-25 |
| K834350 | ACUFEX DREZ COMMUNICATING DRILL GUIDE | Acufex Microsurgical, Inc. | 1984-03-19 |
| K830720 | GRAF MENISCAL SUTURE SET | Acufex Microsurgical, Inc. | 1983-06-16 |
| K821618 | DISPOSABLE NEEDLE HOLDERS | Medcare Products | 1982-06-21 |
| K810888 | BOUNDARY TUBING HOLDERS | The Buckeye Cellulose Corp. | 1981-04-23 |
| K810788 | SURGICAL TUBE HOLDER | The Urology Group | 1981-04-17 |
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