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FDA 510(k)

BASE ONLY, TORONTO CHAIR

K-Number: K832322 · 1983-08-12

Decision Date1983-08-12
Product CodeIQC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BASE ONLY, TORONTO CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Equipment Corp.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832322. The device is classified under product code IQC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BASE ONLY, TORONTO CHAIR?

BASE ONLY, TORONTO CHAIR is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Intl. Medical Equipment Corp.. The 510(k) number is K832322.

When did BASE ONLY, TORONTO CHAIR receive FDA 510(k) clearance?

BASE ONLY, TORONTO CHAIR received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832322.

Who is the listed applicant for BASE ONLY, TORONTO CHAIR?

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

What is the FDA product code for BASE ONLY, TORONTO CHAIR?

The FDA product code for BASE ONLY, TORONTO CHAIR is IQC.

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 Intl. Medical Equipment 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.

Related Devices (Code: IQC)

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

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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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