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FDA 510(k)

CENTIDISC

K-Number: K813524 · 1981-12-31

ApplicantBel-Art Products
Decision Date1981-12-31
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTIDISC is the device name listed in this FDA 510(k) record. The listed applicant is Bel-Art Products. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813524. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTIDISC?

CENTIDISC is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Bel-Art Products. The 510(k) number is K813524.

When did CENTIDISC receive FDA 510(k) clearance?

CENTIDISC received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813524.

Who is the listed applicant for CENTIDISC?

The FDA 510(k) record lists Bel-Art Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTIDISC?

The FDA product code for CENTIDISC is JQC.

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Other records listing Bel-Art Products 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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Related Devices (Code: JQC)

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

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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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