510(k) · Cleared
ClearedIntromit Hand Access Port for Hand Assisted Laparoscopic Surgery, Model FP880-150
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtech, Ltd. · GCJ Laparoscope, General & Plastic Surgery
Cleared on May 27, 1999 after an 87-day review. The FDA summary names its predicate without a number. 5 later devices descend from it.
- Decided
- May 27, 1999
- Review
- 87 days
- Class
- Class II
- Product code
- GCJ
- Recalls
- None
- Predicates
- 0
5 later devices descend from it, 1 citing it directly.
- This deviceK990663 Intromit Hand Access Port for Hand Assisted Laparoscopic Surgery…Medtech, Ltd. · 1999
- Descendant · cites it directly · 4 of its ownK014047 Applied Gelport Laparoscopic Hand Access DeviceApplied Medical Resources Corp. · 2002
- Descendant · 2 generations on · 3 of its ownK090275 Gelport Single Incision Access SystemApplied Medical Resources Corp. · 2009
- Descendant · 2 generations on · 0 of its ownK202688 AFS Medical Sterile Single-Use Access Port SystemAfs Medical Co., Ltd. · 2021
- Descendant · 3 generations on · 0 of its ownK120898 Keyport System, Includes: Keyport Silicone Sealing Insert 8850XXX…Richard Wolf Medical Instruments Corp. · 2012
- Descendant · 3 generations on · 0 of its ownK100180 Surgiquest Anchorport Sil KitSurgiquest, Inc. · 2010
Most influential descendants
Showing 5 of 5 · See all- K014047Applied Gelport Laparoscopic Hand Access DeviceApplied Medical Resources Corp. · 2002 · cites it directly4descendants
- K090275Gelport Single Incision Access SystemApplied Medical Resources Corp. · 2009 · 2 generations on3descendants
- K202688AFS Medical Sterile Single-Use Access Port SystemAfs Medical Co., Ltd. · 2021 · 2 generations on0descendants
- K120898Keyport System, Includes: Keyport Silicone Sealing Insert 8850XXX Keyport Trucar 8850XX…Richard Wolf Medical Instruments Corp. · 2012 · 3 generations on0descendants
- K100180Surgiquest Anchorport Sil KitSurgiquest, Inc. · 2010 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K990663 | Intromit Hand Access Port for Hand Assisted Laparoscopic Surgery, Model… | Medtech, Ltd. | 1999 | — |
| +1 | K014047 | Applied Gelport Laparoscopic Hand Access Device | Applied Medical Resources Corp. | 2002 | — |
| +2 | K090275 | Gelport Single Incision Access System | Applied Medical Resources Corp. | 2009 | — |
| +2 | K202688 | AFS Medical Sterile Single-Use Access Port System | Afs Medical Co., Ltd. | 2021 | — |
| +3 | K120898 | Keyport System, Includes: Keyport Silicone Sealing Insert 8850XXX Keyport… | Richard Wolf Medical Instruments Corp. | 2012 | — |
| +3 | K100180 | Surgiquest Anchorport Sil Kit | Surgiquest, Inc. | 2010 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 1 | 0 |
| 2009 | 1 | 0 |
| 2010 | 1 | 0 |
| 2012 | 1 | 0 |
| 2021 | 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 GCJ? 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 GCJ device
- #1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 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? (6)
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 |
|---|---|---|---|
| * | — | Pilling Weck’s Dexterity® Pneumo Sleeve and Protector® Retractor Named without a submission number | |
| * | — | Karl Storz Endoscopy America, Inc.’s trocars and cannulas for endoscopic and… Named without a submission number | |
| * | — | Solos Endoscopy Inc. GS-4300 Cannula and Trocar and GS-4500 Cannula and Trocar Named without a submission number | |
| * | — | Marlow Surgical Technologies Hasson SAC Cannula Named without a submission number | |
| * | — | Ethicon, Inc.’s Endopath Trocar Named without a submission number | |
| * | — | Innerdyne Medical ‘Step” Radical Expansion Obturator/Cannula Named without a submission number |
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K014047 | Applied Gelport Laparoscopic Hand Access Device | 2002 | 4 |
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?
- Of its descendants, K014047 (Applied Medical Resources Corp., 2002) has gone furthest, with 4 descendants of its own.
How does its category compare?
All GCJ devicesGCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GCJ
21in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GCJ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GCJ
5in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · GCJ
5,860in 2025
MAUDE reports naming product code GCJ, 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 | 18 | 42 | 12 | 1,639 |
| 2008 | 19 | 73 | 16 | 1,319 |
| 2009 | 21 | 85 | 6 | 1,995 |
| 2010 | 24 | 122 | 30 | 2,657 |
| 2011 | 15 | 113 | 9 | 2,133 |
| 2012 | 17 | 88 | 1 | 1,526 |
| 2013 | 15 | 93 | 7 (1) | 1,565 |
| 2014 | 19 | 90 | 2 | 1,714 |
| 2015 | 26 | 76 | 0 | 1,710 |
| 2016 | 27 | 99 | 5 | 2,080 |
| 2017 | 20 | 77 | 1 | 3,468 |
| 2018 | 21 | 88 | 1 | 2,562 |
| 2019 | 15 | 60 | 0 | 2,578 |
| 2020 | 28 | 61 | 0 | 2,618 |
| 2021 | 18 | 116 | 0 | 3,431 |
| 2022 | 20 | 103 | 1 | 3,945 |
| 2023 | 31 | 109 | 1 | 6,002 |
| 2024 | 29 | 90 | 0 | 6,047 |
| 2025 | 21 | 108 | 5 | 5,860 |
| 2026 | 26 | 122 | 1 | — |
What is it indicated for?
The Intromit is inserted into the patient’s abdomen to provide abdominal access for the surgeon’s hand while preserving the peritoneum during laparoscopic 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/K990663 · printed Nov 6, 2026
Cite this page
510(k) Report. “K990663: Intromit Hand Access Port for Hand Assisted Laparoscopic Surgery, Model FP880-150.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K990663
Report an extraction error
Are you the manufacturer?
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