# Namic

- Location (FDA's records): Glens Falls, NY
- FDA decisions: 8 (1979–1996): 8 510(k) clearances
- Product codes: DRS (2), DQO (2), DTL (1), FPA (1), DQY (1), MAV (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 7 (3 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- North American Instrument Corp.: 1 (https://510kreport.com/company/north-american-instrument)

## Firms that cite its devices most
- Cryo Vascular Systems, Inc.: 1 (https://510kreport.com/company/cryo-vascular-systems)
- Coeur, Inc.: 1 (https://510kreport.com/company/coeur)
- Deroyal Industries, Inc.: 1 (https://510kreport.com/company/deroyal-industries)
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)

## Its most-cited devices
- K822100: High Pressure Contrast Injection Line (1982), cited by 2
- K951722: Perceptor Compensator Morse Manifold (1996), cited by 1
- K953676: Breeze Digital Inflation Device (1996), cited by 1

## Recent decisions
- K953676: Breeze Digital Inflation Device (Mar 29, 1996)
- K951722: Perceptor Compensator Morse Manifold (Mar 25, 1996)
- K921322: Morse Anesthesia Manifold (Jul 9, 1993)
- K822100: High Pressure Contrast Injection Line (Aug 24, 1982)
- K813549: Continuous Flush Device (Jan 12, 1982)
- K790082: Arterial Extension Set (Jan 25, 1979)
- K790083: Catheter, Arterial Line (Jan 25, 1979)
- K782095: Stopcocks, Manifolds (Jan 23, 1979)

Source page: https://510kreport.com/company/namic