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FDA 510(k)

GOETTINGER EMERGENCY RESUSCITATION TUBE

K-Number: K892123 · 1989-07-14

ApplicantPlastic Parts Corp.
Decision Date1989-07-14
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GOETTINGER EMERGENCY RESUSCITATION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Plastic Parts Corp.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K892123. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOETTINGER EMERGENCY RESUSCITATION TUBE?

GOETTINGER EMERGENCY RESUSCITATION TUBE is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Plastic Parts Corp.. The 510(k) number is K892123.

When did GOETTINGER EMERGENCY RESUSCITATION TUBE receive FDA 510(k) clearance?

GOETTINGER EMERGENCY RESUSCITATION TUBE received FDA 510(k) clearance on 1989-07-14, under 510(k) number K892123.

Who is the listed applicant for GOETTINGER EMERGENCY RESUSCITATION TUBE?

The FDA 510(k) record lists Plastic Parts Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GOETTINGER EMERGENCY RESUSCITATION TUBE?

The FDA product code for GOETTINGER EMERGENCY RESUSCITATION TUBE is CAE.

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Related Devices (Code: CAE)

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Official Source

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

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