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FDA 510(k)

TREONIC IP5

K-Number: K830936 · 1983-04-12

ApplicantVickers America Medical Corp.
Decision Date1983-04-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TREONIC IP5 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 1983-04-12 under 510(k) number K830936. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREONIC IP5?

TREONIC IP5 is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K830936.

When did TREONIC IP5 receive FDA 510(k) clearance?

TREONIC IP5 received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830936.

Who is the listed applicant for TREONIC IP5?

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 TREONIC IP5?

The FDA product code for TREONIC IP5 is FRN.

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Other records listing Vickers America Medical Corp. 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.

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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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