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)

POWERMATIC EXAMINATION TABLE

K-Number: K933727 · 1994-02-09

ApplicantHausmann Industries, Inc.
Decision Date1994-02-09
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWERMATIC EXAMINATION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Hausmann Industries, Inc.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K933727. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWERMATIC EXAMINATION TABLE?

POWERMATIC EXAMINATION TABLE is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Hausmann Industries, Inc.. The 510(k) number is K933727.

When did POWERMATIC EXAMINATION TABLE receive FDA 510(k) clearance?

POWERMATIC EXAMINATION TABLE received FDA 510(k) clearance on 1994-02-09, under 510(k) number K933727.

Who is the listed applicant for POWERMATIC EXAMINATION TABLE?

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

What is the FDA product code for POWERMATIC EXAMINATION TABLE?

The FDA product code for POWERMATIC EXAMINATION TABLE is INQ.

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: INQ)

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.

K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777Tri W-G, Inc.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, 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.

↑