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FDA 510(k)

DENTAL PLASTIC BITE FORK

K-Number: K892373 · 1989-06-12

ApplicantTexapol Corp.
Decision Date1989-06-12
Product CodeEJP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL PLASTIC BITE FORK is the device name listed in this FDA 510(k) record. The listed applicant is Texapol Corp.. It received FDA 510(k) clearance on 1989-06-12 under 510(k) number K892373. 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 DENTAL PLASTIC BITE FORK?

DENTAL PLASTIC BITE FORK is a medical device that received FDA 510(k) clearance on 1989-06-12. The listed applicant is Texapol Corp.. The 510(k) number is K892373.

When did DENTAL PLASTIC BITE FORK receive FDA 510(k) clearance?

DENTAL PLASTIC BITE FORK received FDA 510(k) clearance on 1989-06-12, under 510(k) number K892373.

Who is the listed applicant for DENTAL PLASTIC BITE FORK?

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

What is the FDA product code for DENTAL PLASTIC BITE FORK?

The FDA product code for DENTAL PLASTIC BITE FORK 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.

K926190ALRAND INC. (DENTAL HAND INSTRUMENTS)Alrand, Inc.K896131GNATHOMAT ARTICULATORIvoclar North America, Inc.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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