# E. R. Squibb & Sons, Inc.

- Location (FDA's records): New York, NY
- FDA decisions: 32 (1977–1982): 32 510(k) clearances
- Product codes: EXB (10), CDP (3), KHQ (2), CDX (2), KNX (2), CGR (2), EXD (1), CGI (1), JLW (1), CIB (1), EZR (1), DPO (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
- Coloplast Corp.: 1 (https://510kreport.com/company/coloplast)

## Its most-cited devices
- K811240: Sur-Fit Loop Ostomy O.R. Set (1981), cited by 1

## Recent decisions
- K821494: Ria Stat 16 (Jun 3, 1982)
- K820616: Angiotensis I-Squibb Radioimmunoassay (Mar 26, 1982)
- K820340: T3 Uptake-Squibb Diagnostic Kit (Mar 4, 1982)
- K820341: Cortisol-Squibb Radioimmunoassay Kit (Mar 4, 1982)
- K811240: Sur-Fit Loop Ostomy O.R. Set (Jun 16, 1981)
- K811239: Sur-Fit Disposable Convex Insert (Jun 9, 1981)
- K811160: Sur-Fit Irrigation Sleeve (Jun 2, 1981)
- K811163: Sur-Fit Disposable Fange Cap (May 21, 1981)

Source page: https://510kreport.com/company/e-r-squibb-sons