# Lifeguard Medical Products, Inc.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 12 (1981–2002): 12 510(k) clearances
- Product codes: CAN (2), BTM (2), BZO (1), BYJ (1), HET (1), BZD (1), GCJ (1), GAD (1), CAH (1), GEI (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
- Engineered Medical Systems: 1 (https://510kreport.com/company/engineered-medical-systems)

## Its most-cited devices
- K881086: Lifeguard Mouth to Mask Resuscitator (1988), cited by 1

## Recent decisions
- K013421: Lifeguard Nasal Cpap Mask and Accessories (Jan 8, 2002)
- K915296: Monopolar Electrode (Sep 3, 1992)
- K920471: Levy Articulating Retractor (Jun 23, 1992)
- K915505: Regulator Flowmeter (Apr 22, 1992)
- K915297: Trocar & Trocar Sleeeve 11MM, 10MM, 8MM & 5MM (Feb 11, 1992)
- K915298: Suction/Irrigation Cannula; Catlog #532.00 (Jan 23, 1992)
- K880958: Lifeguard Bacterial and Viral Filter (Apr 27, 1988)
- K880959: Lifeguard Gas Sampling Line for Mass Spectrometry (Apr 14, 1988)

Source page: https://510kreport.com/company/lifeguard-medical-products