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FDA 510(k)

DINGMAN ZYGOMA ELEVATOR

K-Number: K772399 · 1978-01-17

ApplicantEdward Weck, Inc.
Decision Date1978-01-17
Product CodeKAD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DINGMAN ZYGOMA ELEVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1978-01-17 under 510(k) number K772399. The device is classified under product code KAD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DINGMAN ZYGOMA ELEVATOR?

DINGMAN ZYGOMA ELEVATOR is a medical device that received FDA 510(k) clearance on 1978-01-17. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772399.

When did DINGMAN ZYGOMA ELEVATOR receive FDA 510(k) clearance?

DINGMAN ZYGOMA ELEVATOR received FDA 510(k) clearance on 1978-01-17, under 510(k) number K772399.

Who is the listed applicant for DINGMAN ZYGOMA ELEVATOR?

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

What is the FDA product code for DINGMAN ZYGOMA ELEVATOR?

The FDA product code for DINGMAN ZYGOMA ELEVATOR is KAD.

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Other records listing Edward Weck, 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.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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Related Devices (Code: KAD)

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.

K841356ELEVATORTreace Medical, Inc.K822190ENT ELEVATORSKelleher Corp.K822270VARIOUS TYPES OF ENT ELEVATORSKelleher Corp.K772391BOIES NASAL FRACTURE ELEVATOREdward Weck, 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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