510(k) K792156
- Device
- LANCER SPECIMEN CONTAINER
- Applicant
- SHERWOOD MEDICAL CO.
- 510(k) number
- K792156
- Product code
- FMH
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-12-10
- Date received
- 1979-10-29
- Regulation
- 864.3250
- Classification name
- Container, Specimen, Sterile
- Medical specialty
- Pathology
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 4221 Richmond Rd., NW Walker MI US 49534 49534
FDA Registration Numbers#
- 1123137
- 3000224270
- 3015821396
- 3008717264
- 3007480628
- 3005440795
- 1933015
- 2431166
- 3017231740
- 3017231634
- 3012422258
- 3005595283
- 3030516433
- 3012445205
- 3015967359
- 2530112
- 3009963993
- 1625425
- 2011171
- 9612030
- 1060680
- 1061124
- 3013666218
- 3014159736
- 9680143
- 3012763559
- 9611024
- 3012307300
- 3013337852
- 8040278
- 3015337348
- 3010041511
- 3023443877
- 3007075140
- 2242656
- 3009302820
- 2433012
- 3002444944
- 8010374
- 3005735987
- 3010131137
- 3019387954
- 3009420598
- 9612501
- 9611446
- 3015173212
- 3004111573
- 3007597038
- 3013894805
- 3014437893
- 3021917553
- 3020746799
- 2030624
- 3008449424
- 3004519921
- 3011862887
- 3012797688
- 3038311113
- 3010220595
- 2320762
- 3003917514
- 1054241
- 3015895045
- 1045379
- 3008496560
- 1030489
- 1917413
- 1314344
- 3005690789
- 3027605742
- 3015505238
- 2245590
- 9680836
- 3006673317
- 3008285983
- 3003965134
- 8020315
- 3013187142
- 9616517
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FMH #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K900983 | TRI-TECH URINE SPECIMEN KIT | Tri-Tech, Inc. | 1990-09-17 |
| K823763 | VARIOUS-SPECIMEN COLLECTORS | Cordis Corp. | 1983-01-19 |
| K820180 | CALCULI FILTER CUP | Omnimedical | 1982-02-05 |
| K812933 | LANCER SPECIMEN CONTAINER | Sherwood Medical Co. | 1981-11-06 |
| K802340 | SPECIMEN SET | American Pharmaseal Div. Ahsc | 1980-10-10 |
| K802002 | URINE SPECIMEN CONTAINER #'S 1013-1016 | Pollak (Intl.), Ltd. | 1980-09-09 |
| K800947 | MIDSTREAM COLLECTION KIT | Sage Products, Inc. | 1980-05-30 |
| K800309 | SPECIMEN COLLECTION PAN | Sage Products, Inc. | 1980-02-26 |
| K800233 | ABCO MIDSTREAM URINE COLLECTION SET | Abco Dealers, Inc. | 1980-02-26 |
| K792710 | PARA-PAK CLEAN VIAL | Meridian Diagnostics, Inc. | 1980-01-28 |
| K792211 | SPECIMAN CUP & EMESIS BASIN | General Clinical Plastics Corp. | 1979-11-16 |
| K790915 | JUHN TYM-TAP | Xomed, Inc. | 1979-06-27 |
| K790291 | OPERATING ROOM SPECIMEN CONTAINER | Sage Products, Inc. | 1979-04-10 |
| K781557 | 24-HOUR URINE COLLECTION COOLING WRAP | Sage Products, Inc. | 1978-10-17 |
| K780167 | CATH KIT, URINE SPECIMEN | C.R. Bard, Inc. | 1978-02-21 |
Legacy Summary#
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FDA Review#
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