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FDA 510(k)

CPR GENERAL SURGERY TRAY

K-Number: K960241 · 1996-03-22

ApplicantCustom Pack Reliability
Decision Date1996-03-22
Product CodeLWI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CPR GENERAL SURGERY TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Custom Pack Reliability. It received FDA 510(k) clearance on 1996-03-22 under 510(k) number K960241. The device is classified under product code LWI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR GENERAL SURGERY TRAY?

CPR GENERAL SURGERY TRAY is a medical device that received FDA 510(k) clearance on 1996-03-22. The listed applicant is Custom Pack Reliability. The 510(k) number is K960241.

When did CPR GENERAL SURGERY TRAY receive FDA 510(k) clearance?

CPR GENERAL SURGERY TRAY received FDA 510(k) clearance on 1996-03-22, under 510(k) number K960241.

Who is the listed applicant for CPR GENERAL SURGERY TRAY?

The FDA 510(k) record lists Custom Pack Reliability as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPR GENERAL SURGERY TRAY?

The FDA product code for CPR GENERAL SURGERY TRAY is LWI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Custom Pack Reliability as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960205CPR TRACHEOTOMY CARE TRAYK960243CPR C-SECTION DELIVERY PACKK960239CPR D & C TRAYK960216CPR SUCTION CATHETER KITK960210CPR ORTHO HAND PACKK960206CPR DRESSING CHANGE TRAY

View all 21 devices →

Related Devices (Code: LWI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960421SINUSCAN 102/SINUSPRINTFerguson MedicalK960044ULTRAMAX/MODEL NUMBER A1Entlab OYK874081ENTERSCANPie Data Medical BV

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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