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)

TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP

K-Number: K925181 · 1993-02-05

ApplicantTechmedica, Inc.
Decision Date1993-02-05
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1993-02-05 under 510(k) number K925181. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP?

TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is Techmedica, Inc.. The 510(k) number is K925181.

When did TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP receive FDA 510(k) clearance?

TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP received FDA 510(k) clearance on 1993-02-05, under 510(k) number K925181.

Who is the listed applicant for TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP?

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

What is the FDA product code for TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP?

The FDA product code for TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP is JDL.

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 Techmedica, 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.

K933935CKS POROUS COATED FEMORAL COMPONENTK932017TECHMEDICA CONTINUUM HIP WITH HA COATINGK931929TECHMEDICA CONTINUUM HIP SYSTEMK926387TECHMEDICA STANDARD CEMENTED HIP SYSTEMK925420TECHMEDICA STANDARD BIPOLAR SYSTEMK923808MULLER STRAIGHT STEM FEMORAL PROSTHESIS

View all 31 devices →

Related Devices (Code: JDL)

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.

K073499VERSYS EPOCH FULLCOAT HIP PROSTHESIS, MODEL 4088 SERIESZimmer, Inc.K070785DYNASTY ACETABULAR SYSTEMWrightmedicaltechnologyincK061844DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINERWrightmedicaltechnologyincK051995PROFEMUR RENAISSANCE HIP STEMWrightmedicaltechnologyincK051348CONSERVE TOTAL FEMORAL HEADWrightmedicaltechnologyincK042841M2A/C2A ACETABULAR SYSTEMBiomet, 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.

↑