ANALOR FOUR-DENTAL MODEL
K-Number: K801100 · 1980-05-28
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Device Summary
Frequently Asked Questions
What is the ANALOR FOUR-DENTAL MODEL?
ANALOR FOUR-DENTAL MODEL is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is Narco Mckesson Co.. The 510(k) number is K801100.
When did ANALOR FOUR-DENTAL MODEL receive FDA 510(k) clearance?
ANALOR FOUR-DENTAL MODEL received FDA 510(k) clearance on 1980-05-28, under 510(k) number K801100.
Who is the listed applicant for ANALOR FOUR-DENTAL 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 ANALOR FOUR-DENTAL MODEL?
The FDA product code for ANALOR FOUR-DENTAL 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
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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