# Interspec, Inc.

- Location (FDA's records): Ambler, PA
- FDA decisions: 17 (1982–1994): 17 510(k) clearances
- Product codes: ITX (6), JOP (3), DXK (2), IYO (2), GWQ (1), GWK (1), DPT (1), DPW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Shantou Institute of Ultrasonic Instuments: 1 (https://510kreport.com/company/shantou-institute-of-ultrasonic-instuments)

## Its most-cited devices
- K924231: Interspec Apogee Cla (1993), cited by 1

## Recent decisions
- K940671: Interspec Apogee RX400 Ultrasound Imaging System and Doppler Ultrasound Flowmeter (Nov 22, 1994)
- K924231: Interspec Apogee Cla (Jun 14, 1993)
- K915696: Interspec Apogee Endo-V Probe and Needle Guide (Nov 24, 1992)
- K920678: Ultrasound Imagaing System and Doppler  Flowmeter (Apr 2, 1992)
- K911073: Probe Refill Kit (Jun 6, 1991)
- K910049: Interspec Apogee, Modification (Apr 29, 1991)
- K903839: Interspec Apogee (Nov 16, 1990)
- K900155: Interspec 2 MHZ, Transcranial Pulsed Wave Doppler (Oct 5, 1990)

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