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FDA 510(k)

COMPALOR-ORAL SURGERY MODEL

K-Number: K801102 · 1980-06-17

Decision Date1980-06-17
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPALOR-ORAL SURGERY MODEL is the device name listed in this FDA 510(k) record. The listed applicant is Narco Mckesson Co.. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K801102. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPALOR-ORAL SURGERY MODEL?

COMPALOR-ORAL SURGERY MODEL is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Narco Mckesson Co.. The 510(k) number is K801102.

When did COMPALOR-ORAL SURGERY MODEL receive FDA 510(k) clearance?

COMPALOR-ORAL SURGERY MODEL received FDA 510(k) clearance on 1980-06-17, under 510(k) number K801102.

Who is the listed applicant for COMPALOR-ORAL SURGERY MODEL?

The FDA 510(k) record lists Narco Mckesson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPALOR-ORAL SURGERY MODEL?

The FDA product code for COMPALOR-ORAL SURGERY MODEL is BSZ.

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 Narco Mckesson Co. 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: BSZ)

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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