# K102048: Atraumatic Vascular Clamps

- Pathway: 510(k) (Traditional)
- Applicant: Geomed Medizin-Technik GmbH & Co. KG
- Decided: Nov 9, 2010 after 111 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: 1 (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. The FDA summary names its predicate without a number.
- (no number) Aesculap Inc. Vascular Clamps: named in the summary without a submission number

## Recalls of this device
- Aug 7, 2019 · Class II · Z-2435-2019: A small crack at the box lock corner may after multiple cleaning and sterilization cycles produce an increased risk of corrosion, weakening the instrument and resulting in premature need for replaceme

## Indications for use
GEOMED Vascular Clamps are intended for use for temporary occlusion of blood vessels during surgical procedures.

Source page: https://510kreport.com/device/K102048
Methodology: https://510kreport.com/methodology