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FDA 510(k)

CPR SUCTION CATHETER KIT

K-Number: K960216 · 1996-04-15

Decision Date1996-04-15
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CPR SUCTION CATHETER KIT 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 1996-04-15 under 510(k) number K960216. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR SUCTION CATHETER KIT?

CPR SUCTION CATHETER KIT is a medical device that received FDA 510(k) clearance on 1996-04-15. The listed applicant is Custom Pack Reliability. The 510(k) number is K960216.

When did CPR SUCTION CATHETER KIT receive FDA 510(k) clearance?

CPR SUCTION CATHETER KIT received FDA 510(k) clearance on 1996-04-15, under 510(k) number K960216.

Who is the listed applicant for CPR SUCTION CATHETER KIT?

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 SUCTION CATHETER KIT?

The FDA product code for CPR SUCTION CATHETER KIT is JOL.

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.

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.

View all 21 devices →

Related Devices (Code: JOL)

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.

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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