FDA 510(k)

DAY EAR HOOK

K-Number: K772390 · 1978-01-17

Decision Date1978-01-17

Product CodeJYL

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

DAY EAR HOOK 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 K772390. The device is classified under product code JYL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAY EAR HOOK?

DAY EAR HOOK 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 K772390.

When did DAY EAR HOOK receive FDA 510(k) clearance?

DAY EAR HOOK received FDA 510(k) clearance on 1978-01-17, under 510(k) number K772390.

Who is the listed applicant for DAY EAR HOOK?

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 DAY EAR HOOK?

The FDA product code for DAY EAR HOOK is JYL.

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 TROCAR K914690LM15(TM), CATALOG NUMBER - 523821 K911915HEMOCLIP II K914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705 K902108HEM-O-LOK(TM)

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Related Devices (Code: JYL)

K834188JAKOBI SURG. INSTRUMENTS #7 10/43Imm Enterprises , Ltd.K822195MIRCOSURGICAL INSTRUMENTSKelleher Corp.K822166MICROSURGICAL EAR HOOKKelleher Corp.K780287DAY HEAR HOOKEdward Weck, 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.