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FDA 510(k)

FACEBOW FOR BALANCE ARTICULATOR

K-Number: K830775 · 1983-04-28

ApplicantAlmore Intl., Inc.
Decision Date1983-04-28
Product CodeKCR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FACEBOW FOR BALANCE ARTICULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Almore Intl., Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830775. The device is classified under product code KCR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FACEBOW FOR BALANCE ARTICULATOR?

FACEBOW FOR BALANCE ARTICULATOR is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Almore Intl., Inc.. The 510(k) number is K830775.

When did FACEBOW FOR BALANCE ARTICULATOR receive FDA 510(k) clearance?

FACEBOW FOR BALANCE ARTICULATOR received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830775.

Who is the listed applicant for FACEBOW FOR BALANCE ARTICULATOR?

The FDA 510(k) record lists Almore Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FACEBOW FOR BALANCE ARTICULATOR?

The FDA product code for FACEBOW FOR BALANCE ARTICULATOR is KCR.

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Other records listing Almore Intl., Inc. 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.

K862851ALMORE FACE MASKK854692MONARCH II BLEACHING INSTRUMENTK854696OP II VISIBLE LIGHT CURING SYSTEMK854690DIAMONDS BURS-COMPOSIT FINISHINGK854691DIAMOND BURS-HANDPIECEK854700EZ-ON TUBING CONDITIONER (LUBRICANT)

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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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