CPR GENERAL SURGERY TRAY— 510(k) K960241

Name: FDA 510(k) clearance K960241
Creator: U.S. Food and Drug Administration
Published: 1996-03-22

Substantially Equivalent

Custom Pack Reliability

FDA 510(k) clearance K960241 for CPR GENERAL SURGERY TRAY, Substantially Equivalent on 1996-03-22. Applicant: Custom Pack Reliability. Device class: 2.

Clearance details

Applicant: Custom Pack Reliability
Product code: Code LWI
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 1996-01-16
Decision date: 1996-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orlando, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LWI

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K960421 — SINUSCAN 102/SINUSPRINT1997-04-16
K960044 — ULTRAMAX/MODEL NUMBER A11996-08-02
K874081 — ENTERSCAN1987-12-31

More clearances from Custom Pack Reliability

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K960205 — CPR TRACHEOTOMY CARE TRAY1996-08-27
K960239 — CPR D & C TRAY1996-05-23
K960243 — CPR C-SECTION DELIVERY PACK1996-05-23
K960216 — CPR SUCTION CATHETER KIT1996-04-15
K960206 — CPR DRESSING CHANGE TRAY1996-04-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.