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FDA 510(k)

FORCEPS, STYLE #849

K-Number: K771522 · 1977-08-16

ApplicantPremier Dental Products Co.
Decision Date1977-08-16
Product CodeEMH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FORCEPS, STYLE #849 is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Products Co.. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771522. The device is classified under product code EMH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, STYLE #849?

FORCEPS, STYLE #849 is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is Premier Dental Products Co.. The 510(k) number is K771522.

When did FORCEPS, STYLE #849 receive FDA 510(k) clearance?

FORCEPS, STYLE #849 received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771522.

Who is the listed applicant for FORCEPS, STYLE #849?

The FDA 510(k) record lists Premier Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEPS, STYLE #849?

The FDA product code for FORCEPS, STYLE #849 is EMH.

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 Premier Dental Products 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.

K132526KNIT-PAK+K131212PREMIER CERAMIC PRIMERK083695TRAXODENTK062683ENAMEL PRO VARNISHK062166ENAMEL PROK061997PREMIER SELF-ETCHING ENAMEL SEALANT

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Related Devices (Code: EMH)

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.

K890256BONE RONGEUR, DOUBLE-ACTIONKinetic Medical ProductsK890255BONE RONGEUR, SINGLE-ACTIONKinetic Medical ProductsK854887MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLATWalter Lorenz Surgical, Inc.K851710586 TO 596 VARIOUS TYPES DENTAL ROOT SPLINTER FORCArtiberiaK834190JAKOBI SURG. INSTRUMENTS #8 15Imm Enterprises , Ltd.K834366SURGICAL INSTRUMENTS & ACCESSORIESC.B.S. Biotechnics, Inc.

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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