510(k) · Cleared
ClearedOscar Bipolar Scissors and Oscar Bipolar Reusable Cartridges
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Enable Medical Corp. · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Jun 29, 1998 as substantially equivalent to K951387 (Symbiosis Corp., 1995) and 6 other predicates after an 87-day review. Its family tree reaches back 2 generations to 1994. 8 later devices descend from it.
- Decided
- Jun 29, 1998
- Review
- 87 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 7
Its longest line of descent runs back 2 generations to K945975 (1994). 7 ancestors in all. 8 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK945975 Evershears (R) Scissors, Bilap (R) Probes, Bicoag (R) ForcepsEverest Medical Corp. · 1994
- 1 generation backK972558 Bipolar ScissorsEnable Medical Corp. · 1997
- This deviceK981219 Oscar Bipolar Scissors and Oscar Bipolar Reusable CartridgesEnable Medical Corp. · 1998
- Descendant · cites it directly · 7 of its ownK992996 Enable Endoscopic Bipolar ScissorsEnable Medical Corp. · 1999
- Descendant · 2 generations on · 6 of its ownK001330 Sovereign Bipolar InstrumentsAesculap, Inc. · 2000
- Descendant · 3 generations on · 3 of its ownK030890 SwitchbladeSnowden Pencer, Inc. · 2003
- Descendant · 4 generations on · 1 of its ownK113407 Snowden Pencer Laparoscopic Ergonomic Reposable ScissorsCarefusion 2200, Inc. · 2012
- Descendant · 3 generations on · 0 of its ownK160393 AdTecAesculap, Inc. · 2016
Showing 5 of 8 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 8 · See all- K992996Enable Endoscopic Bipolar ScissorsEnable Medical Corp. · 1999 · cites it directly7descendants
- K001330Sovereign Bipolar InstrumentsAesculap, Inc. · 2000 · 2 generations on6descendants
- K030890SwitchbladeSnowden Pencer, Inc. · 2003 · 3 generations on3descendants
- K113407Snowden Pencer Laparoscopic Ergonomic Reposable ScissorsCarefusion 2200, Inc. · 2012 · 4 generations on1descendant
- K160393AdTecAesculap, Inc. · 2016 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K945975 | Evershears (R) Scissors, Bilap (R) Probes, Bicoag (R) Forceps | Everest Medical Corp. | 1994 | — |
| −1 | K972558 | Bipolar Scissors | Enable Medical Corp. | 1997 | — |
| 0 (this device) | K981219 | Oscar Bipolar Scissors and Oscar Bipolar Reusable Cartridges | Enable Medical Corp. | 1998 | — |
| +1 | K992996 | Enable Endoscopic Bipolar Scissors | Enable Medical Corp. | 1999 | — |
| +2 | K001330 | Sovereign Bipolar Instruments | Aesculap, Inc. | 2000 | — |
| +3 | K030890 | Switchblade | Snowden Pencer, Inc. | 2003 | — |
| +4 | K113407 | Snowden Pencer Laparoscopic Ergonomic Reposable Scissors | Carefusion 2200, Inc. | 2012 | — |
| +3 | K160393 | AdTec | Aesculap, Inc. | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 2 | 0 |
| 1996 | 1 | 0 |
| 1997 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1999 | 1 | 0 |
| 2000 | 1 | 0 |
| 2003 | 1 | 0 |
| 2008 | 1 | 0 |
| 2012 | 2 | 0 |
| 2013 | 1 | 0 |
| 2016 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in GEI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new GEI device
- #1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 21 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (7)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K951387 | Symbiosis Bipolar ScissorsSummary page 1…Disposable Cartridges Generic/Common Name: Electrosurgical cutting and coagulation device and accessories 21CFR878.4400 PREDICATED DEVICES 1. Symbiosis Bipolar Scissors (K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. Eth… | 1995 |
| * | K945975 | Evershears (R) Scissors, Bilap (R) Probes, Bicoag (R) ForcepsSummary page 1…ctrosurgical cutting and coagulation device and accessories 21CFR878.4400 PREDICATED DEVICES 1. Symbiosis Bipolar Scissors (K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. Ethicon PowerStar Bipolar Scissors (K960476 and K… | 1994 |
| * | K955001 | Evershears Scissors, Bilap Probes, Bicoag ForcepsSummary page 1…cutting and coagulation device and accessories 21CFR878.4400 PREDICATED DEVICES 1. Symbiosis Bipolar Scissors (K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. Ethicon PowerStar Bipolar Scissors (K960476 and K973173) 5. E… | 1995 |
| * | K963930 | CTS Midcab/SVH Bipolar ScissorsSummary page 1…EDICATED DEVICES 1. Symbiosis Bipolar Scissors (K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. Ethicon PowerStar Bipolar Scissors (K960476 and K973173) 5. ENABLE Bipolar Scissors (K972558) 24 ENABLE Medi… | 1997 |
| * | K960476 | Ethicon Bipolar Scissors and Accessory CableSummary page 1…K951387) 2. Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. Ethicon PowerStar Bipolar Scissors (K960476 and K973173) 5. ENABLE Bipolar Scissors (K972558) 24 ENABLE Medical Corporation OSCAR™ Bipolar Scissors 510(k)… | 1996 |
| * | K973173 | Powerstar Bipolar ScissorsSummary page 1…Everest Medical Bipolar Scissors (K945975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. Ethicon PowerStar Bipolar Scissors (K960476 and K973173) 5. ENABLE Bipolar Scissors (K972558) 24 ENABLE Medical Corporation OSCAR™ Bipolar Scissors 510(k) INTENDED USE… | 1997 |
| * | K972558 | Bipolar ScissorsSummary page 1…5975 and K955001) 3. CardioThoracic Systems MIDCAB/SVH Bipolar Scissors (K963930) 4. Ethicon PowerStar Bipolar Scissors (K960476 and K973173) 5. ENABLE Bipolar Scissors (K972558) 24 ENABLE Medical Corporation OSCAR™ Bipolar Scissors 510(k) INTENDED USE The OSCAR™ Bipolar Scissors with OS… | 1997 |
What descends from it? (8)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K992996 | Enable Endoscopic Bipolar Scissors | 1999 | 7 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 4 years and passes through 2 companies; a new generation was cleared every 2.8 years on median.
- None of the 7 ancestors has a recall.
- Of its descendants, K992996 (Enable Medical Corp., 1999) has gone furthest, with 7 descendants of its own.
- 3 other devices also cite its predicate K951387.
How does its category compare?
All GEI devicesGEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GEI
52in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GEI
113in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GEI
4in 2025
Class I (14 since 2007) Class II/III not classified
Adverse event reports per year · GEI
7,592in 2025
MAUDE reports naming product code GEI, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 50 | 51 | 21 | 2,795 |
| 2008 | 61 | 71 | 19 | 2,556 |
| 2009 | 42 | 130 | 27 | 3,591 |
| 2010 | 46 | 109 | 51 | 3,377 |
| 2011 | 35 | 135 | 32 | 4,463 |
| 2012 | 39 | 133 | 30 | 5,216 |
| 2013 | 48 | 136 | 13 | 4,897 |
| 2014 | 49 | 103 | 3 | 4,908 |
| 2015 | 47 | 123 | 4 | 4,936 |
| 2016 | 64 | 108 | 3 | 5,616 |
| 2017 | 52 | 72 | 2 | 6,073 |
| 2018 | 47 | 93 | 6 | 6,545 |
| 2019 | 48 | 93 | 5 | 7,067 |
| 2020 | 59 | 105 | 1 | 6,490 |
| 2021 | 46 | 146 | 6 | 6,354 |
| 2022 | 55 | 150 | 49 | 6,103 |
| 2023 | 65 | 104 | 27 (4) | 7,176 |
| 2024 | 59 | 125 | 22 (10) | 7,897 |
| 2025 | 52 | 113 | 4 | 7,592 |
| 2026 | 43 | 183 | 8 | — |
What is it indicated for?
The OSCAR™ Bipolar Scissors with OSCAR™ Bipolar Disposable Cartridges is intended to cut tissue and control bleeding through coagulation during open surgical procedures and in general surgery.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K981219 · printed Nov 6, 2026
Cite this page
510(k) Report. “K981219: Oscar Bipolar Scissors and Oscar Bipolar Reusable Cartridges.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K981219
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026