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FDA 510(k)

CONVERSE-GILLIES NEEDLE HOLDER

K-Number: K772388 · 1978-01-20

ApplicantEdward Weck, Inc.
Decision Date1978-01-20
Product CodeHXK
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONVERSE-GILLIES NEEDLE HOLDER 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 1978-01-20 under 510(k) number K772388. The device is classified under product code HXK. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERSE-GILLIES NEEDLE HOLDER?

CONVERSE-GILLIES NEEDLE HOLDER is a medical device that received FDA 510(k) clearance on 1978-01-20. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772388.

When did CONVERSE-GILLIES NEEDLE HOLDER receive FDA 510(k) clearance?

CONVERSE-GILLIES NEEDLE HOLDER received FDA 510(k) clearance on 1978-01-20, under 510(k) number K772388.

Who is the listed applicant for CONVERSE-GILLIES NEEDLE HOLDER?

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 CONVERSE-GILLIES NEEDLE HOLDER?

The FDA product code for CONVERSE-GILLIES NEEDLE HOLDER is HXK.

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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: HXK)

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.

K890167HOLDER, NEEDLEDhason Brothers, Inc.K872989MICRINS NEEDLE HOLDERMicrins Surgical, Inc.K860018FISCHER WIRE/PIN CLAMPBuckman Co., Inc.K801594ACE FISCHER EXTERNAL FIXATION DEVICEAce Orthopedic Manufacturing Co.

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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