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FDA 510(k)

ALRAND INC. (DENTAL HAND INSTRUMENTS)

K-Number: K926190 · 1994-01-18

ApplicantAlrand, Inc.
Decision Date1994-01-18
Product CodeEJP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALRAND INC. (DENTAL HAND INSTRUMENTS) is the device name listed in this FDA 510(k) record. The listed applicant is Alrand, Inc.. It received FDA 510(k) clearance on 1994-01-18 under 510(k) number K926190. The device is classified under product code EJP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALRAND INC. (DENTAL HAND INSTRUMENTS)?

ALRAND INC. (DENTAL HAND INSTRUMENTS) is a medical device that received FDA 510(k) clearance on 1994-01-18. The listed applicant is Alrand, Inc.. The 510(k) number is K926190.

When did ALRAND INC. (DENTAL HAND INSTRUMENTS) receive FDA 510(k) clearance?

ALRAND INC. (DENTAL HAND INSTRUMENTS) received FDA 510(k) clearance on 1994-01-18, under 510(k) number K926190.

Who is the listed applicant for ALRAND INC. (DENTAL HAND INSTRUMENTS)?

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

What is the FDA product code for ALRAND INC. (DENTAL HAND INSTRUMENTS)?

The FDA product code for ALRAND INC. (DENTAL HAND INSTRUMENTS) is EJP.

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Related Devices (Code: EJP)

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.

K896131GNATHOMAT ARTICULATORIvoclar North America, Inc.K892373DENTAL PLASTIC BITE FORKTexapol Corp.K884418PREMIER DIE-TRAK ARTICULATORPremier MedicalK872943DISPOSABLE ARTICULATORDentsply Intl.K863009GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEXSds Dental, Inc.K854702PLASTIC MOUNTING RINGSAlmore Intl., Inc.

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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