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)

MARTIN PELVIC LIFT

K-Number: K823206 · 1983-04-28

ApplicantMartin Pelvic Lift Co.
Decision Date1983-04-28
Product CodeFSA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MARTIN PELVIC LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Martin Pelvic Lift Co.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K823206. The device is classified under product code FSA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN PELVIC LIFT?

MARTIN PELVIC LIFT is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Martin Pelvic Lift Co.. The 510(k) number is K823206.

When did MARTIN PELVIC LIFT receive FDA 510(k) clearance?

MARTIN PELVIC LIFT received FDA 510(k) clearance on 1983-04-28, under 510(k) number K823206.

Who is the listed applicant for MARTIN PELVIC LIFT?

The FDA 510(k) record lists Martin Pelvic Lift Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARTIN PELVIC LIFT?

The FDA product code for MARTIN PELVIC LIFT is FSA.

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

Related Devices (Code: FSA)

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.

K942807SURGICAL LIFT SHEETSurgin Surgical Instrumentation, Inc.K930625SANITAS PATIENT LIFTDutton-Lainson Co.K902141ANOLIFT - PORTABLE & ANOLIFT - GANTRYAnodyne Corp.K860837HOYER ONE-TOUCH POWER LIFTERTed Hoyer & Co., Inc.K851844MOLIFTMadshus A/SK844976MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFTMedi-Man Rehabilitation Products, 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.

↑