Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD

K-Number: K890162 · 1989-02-13

ApplicantDhason Brothers, Inc.
Decision Date1989-02-13
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD 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 1989-02-13 under 510(k) number K890162. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD?

EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Dhason Brothers, Inc.. The 510(k) number is K890162.

When did EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD receive FDA 510(k) clearance?

EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD received FDA 510(k) clearance on 1989-02-13, under 510(k) number K890162.

Who is the listed applicant for EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD?

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 EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD?

The FDA product code for EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD is LXH.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 HEADK890165FORCEPS-ORTHOPEDICK890164HUDSON BRACE W/BURRSK890168RETRACTOR, SELF-RETAININGK890166RONGUER-ORTHOPEDICK890161THOMPSON TYPE RASP W/TOMMY BAR

View all 14 devices →

Related Devices (Code: LXH)

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.

K192873SX-One MicroKnifeSonex Health, Inc.K101609SELF RETAINING SOFT TISSUE RETRACTORKoros USA, Inc.K001507MICROPERFORATION INSTRUMENTSmith & Nephew, Inc.K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMOrthopedic Systems, Inc.K943873ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SYOrthomet, Inc.K944188SPINAL MARKERLeibinger L.P.

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.

↑