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FDA 510(k)

HOLDER, NEEDLE

K-Number: K890167 · 1989-02-03

ApplicantDhason Brothers, Inc.
Decision Date1989-02-03
Product CodeHXK
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOLDER, NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Dhason Brothers, Inc.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K890167. 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 HOLDER, NEEDLE?

HOLDER, NEEDLE is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Dhason Brothers, Inc.. The 510(k) number is K890167.

When did HOLDER, NEEDLE receive FDA 510(k) clearance?

HOLDER, NEEDLE received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890167.

Who is the listed applicant for HOLDER, NEEDLE?

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

What is the FDA product code for HOLDER, NEEDLE?

The FDA product code for HOLDER, NEEDLE is HXK.

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Other records listing Dhason Brothers, 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.

K890156IMPACTOR FOR FEMORAL HEADK890162EXTRACTOR FOR AUSTIN MOORE FEMORAL HEADK890165FORCEPS-ORTHOPEDICK890164HUDSON BRACE W/BURRSK890168RETRACTOR, SELF-RETAININGK890161THOMPSON TYPE RASP W/TOMMY BAR

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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.

K872989MICRINS NEEDLE HOLDERMicrins Surgical, Inc.K860018FISCHER WIRE/PIN CLAMPBuckman Co., Inc.K801594ACE FISCHER EXTERNAL FIXATION DEVICEAce Orthopedic Manufacturing Co.K772388CONVERSE-GILLIES NEEDLE HOLDEREdward 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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