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)

ACETABULAR CEMENT COMPRESSOR

K-Number: K813094 · 1981-11-20

ApplicantRichard'S Medical Equip., Inc.
Decision Date1981-11-20
Product Code
DecisionSubstantially Equivalent

Device Summary

ACETABULAR CEMENT COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1981-11-20 under 510(k) number K813094. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETABULAR CEMENT COMPRESSOR?

ACETABULAR CEMENT COMPRESSOR is a medical device that received FDA 510(k) clearance on 1981-11-20. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K813094.

When did ACETABULAR CEMENT COMPRESSOR receive FDA 510(k) clearance?

ACETABULAR CEMENT COMPRESSOR received FDA 510(k) clearance on 1981-11-20, under 510(k) number K813094.

Who is the listed applicant for ACETABULAR CEMENT COMPRESSOR?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Richard'S Medical Equip., 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.

K830793PATIENT GUIDED ELBOW & SHOULDER EXERCK823837RMC TOTAL KNEE SYSTEMK823723SPECTRON PROXIMAL FEMORAL PROSTHESISK823724SPECTRON NECK REPLACEMENT PROSTHESISK823726SPECTRON CONVERSION ENDOPROSTHESIS CUPK823722SPECTRON LONG, STRAIGHT FEMORAL PROSTHES

View all 48 devices →

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.

↑