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FDA 510(k)

COMPALOR-DENTAL MODEL

K-Number: K801103 · 1980-05-28

ApplicantNarco Mckesson Co.
Decision Date1980-05-28
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPALOR-DENTAL 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 1980-05-28 under 510(k) number K801103. 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-DENTAL MODEL?

COMPALOR-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 K801103.

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

COMPALOR-DENTAL MODEL received FDA 510(k) clearance on 1980-05-28, under 510(k) number K801103.

Who is the listed applicant for COMPALOR-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 COMPALOR-DENTAL MODEL?

The FDA product code for COMPALOR-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.

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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.

K801101ANALOR FOUR-ORAL SURGERY MODELK801102COMPALOR-ORAL SURGERY MODELK801100ANALOR FOUR-DENTAL MODELK790456SERIES 7000K781492SERIES 7000 GAS MACHINE

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.

K253330A5 Anesthesia System (A5); A7 Anesthesia System (A7)Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K252746Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL)Drägerwerk AG Co. KgaaK251352Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-700i and related 610i, 620i, 630i series enabled to retrofit RFID features); Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-1, SLS XXX, Multiple Models Pending Configuration)Codonics.IncorporatedK230931AtlanDrägerwerk AG Co. KgaaK213867Carestation 750/750cDatex-Ohmeda, Inc.K201957A8, A9 Anesthesia SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.

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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