# K883790: Surgical Clamp Inserts

- Pathway: 510(k) (Traditional)
- Applicant: Applied Vascular Devices, Inc.
- Decided: Dec 27, 1988 after 111 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Mar 7, 2011 · Not classified · Z-3006-2011: The recall was initiated because Applied Medical has confirmed that Surgical Clamp Inserts, Model Numbers: G-8600, G-8650, G-8655, has the potential packaging nonconformance which could result in a co
- Mar 7, 2011 · Not classified · Z-3004-2011: The recall was initiated because Applied Medical has confirmed that Surgical Clamp Inserts, Model Numbers: G-8600, G-8650, G-8655, has the potential packaging nonconformance which could result in a co
- Mar 7, 2011 · Not classified · Z-3005-2011: The recall was initiated because Applied Medical has confirmed that Surgical Clamp Inserts, Model Numbers: G-8600, G-8650, G-8655, has the potential packaging nonconformance which could result in a co

Source page: https://510kreport.com/device/K883790
Methodology: https://510kreport.com/methodology