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FDA 510(k)

MODEL 114 TREONIC H150 HAEMOHEATER

K-Number: K790936 · 1979-09-04

ApplicantVickers America Medical Corp.
Decision Date1979-09-04
Product CodeKZL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MODEL 114 TREONIC H150 HAEMOHEATER is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1979-09-04 under 510(k) number K790936. The device is classified under product code KZL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 114 TREONIC H150 HAEMOHEATER?

MODEL 114 TREONIC H150 HAEMOHEATER is a medical device that received FDA 510(k) clearance on 1979-09-04. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K790936.

When did MODEL 114 TREONIC H150 HAEMOHEATER receive FDA 510(k) clearance?

MODEL 114 TREONIC H150 HAEMOHEATER received FDA 510(k) clearance on 1979-09-04, under 510(k) number K790936.

Who is the listed applicant for MODEL 114 TREONIC H150 HAEMOHEATER?

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

What is the FDA product code for MODEL 114 TREONIC H150 HAEMOHEATER?

The FDA product code for MODEL 114 TREONIC H150 HAEMOHEATER is KZL.

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Other records listing Vickers America Medical Corp. as applicant

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Related Devices (Code: KZL)

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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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