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#
- 3010131137
- 3004122598
- 1319639
- 3015276780
- 3016710934
- 9612030
- 3015277818
- 3004496839
- 3011862887
- 3012422258
- 1644312
- 2320762
- 3004125670
- 3005327291
- 3007135420
- 3011707784
- 9613662
- 1045379
- 3004519921
- 3011777678
- 3012568936
- 3002444944
- 3044186618
- 1524213
- 3044150131
- 3045058049
- 2028046
- 3017231634
- 3014437893
- 1933015
- 3014637079
- 3015821396
- 3005735987
- 3017231740
- 3003528228
- 3021917553
- 1649518
- 3015134755
- 3003965134
- 3011689956
- 3005012805
- 3010041511
- 9680836
- 9610649
- 2183416
- 3012445205
- 3006082230
- 3011137372
- 3021169869
- 3002907620
- 1219913
- 8010374
- 1125230
- 3000268902
- 3008328679
- 3012421607
- 9611102
- 2029015
- 2951231
- 3012439152
- 3003895930
- 3004127962
- 2244900
- 1210083
- 3012302888
- 1319660
- 2030624
- 2411512
- 3031233007
- 3003824562
- 1921846
- 1054657
- 1422598
- 8020315
- 3017041963
- 3013517171
- 2025773
- 3005739529
- 1528319
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 |
| K800233 | ABCO MIDSTREAM URINE COLLECTION SET | Abco Dealers, Inc. | 1980-02-26 |
| K800309 | SPECIMEN COLLECTION PAN | Sage Products, 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 |
| K780057 | URINE SAMPLE COLLECTION KIT | C.R. Bard, Inc. | 1978-02-21 |
Legacy Summary#
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FDA Review#
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