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FDA 510(k)

BEACH GINGIVAL RETRACTION INSTR. TYPE B

K-Number: K821784 · 1982-07-06

ApplicantPacific Dental Corp.
Decision Date1982-07-06
Product CodeEIG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEACH GINGIVAL RETRACTION INSTR. TYPE B is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Dental Corp.. It received FDA 510(k) clearance on 1982-07-06 under 510(k) number K821784. The device is classified under product code EIG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEACH GINGIVAL RETRACTION INSTR. TYPE B?

BEACH GINGIVAL RETRACTION INSTR. TYPE B is a medical device that received FDA 510(k) clearance on 1982-07-06. The listed applicant is Pacific Dental Corp.. The 510(k) number is K821784.

When did BEACH GINGIVAL RETRACTION INSTR. TYPE B receive FDA 510(k) clearance?

BEACH GINGIVAL RETRACTION INSTR. TYPE B received FDA 510(k) clearance on 1982-07-06, under 510(k) number K821784.

Who is the listed applicant for BEACH GINGIVAL RETRACTION INSTR. TYPE B?

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

What is the FDA product code for BEACH GINGIVAL RETRACTION INSTR. TYPE B?

The FDA product code for BEACH GINGIVAL RETRACTION INSTR. TYPE B is EIG.

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Other records listing Pacific Dental Corp. 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.

K821782BEACH ANESTHETIC SYRINGE CARTR. TYPEK821779BEACH AMALGAM CARRIER, GUN TYPEK821789BEACH CURETTE NO. 2 AND NO. 3 T.G.K821777BEACH MOUTH MIRRORK821778BEACH DRESSING PLIERK821780BEACH EXPLORER NO. 23T.G.

View all 22 devices →

Related Devices (Code: EIG)

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.

K971284OPALDAMUltradent Products, Inc.K854711FIBRELIGHT ILLUMINATING ORAL RETRACTORSDowns Surgical , Ltd.K832366ZOLLER BURNED LIP CONFORMERUniversal Prosthetics, Inc.K771973GINGITRACTDen-Mat Corp.K771399LIP & CHEEK RETRACTORL.D. Caulk Co.K761024RACESTYPTINE RINGSSeptodont, 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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