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)

REHABILITATION TABLES

K-Number: K854947 · 1986-01-03

ApplicantI-Rep, Inc.
Decision Date1986-01-03
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REHABILITATION TABLES is the device name listed in this FDA 510(k) record. The listed applicant is I-Rep, Inc.. It received FDA 510(k) clearance on 1986-01-03 under 510(k) number K854947. 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 REHABILITATION TABLES?

REHABILITATION TABLES is a medical device that received FDA 510(k) clearance on 1986-01-03. The listed applicant is I-Rep, Inc.. The 510(k) number is K854947.

When did REHABILITATION TABLES receive FDA 510(k) clearance?

REHABILITATION TABLES received FDA 510(k) clearance on 1986-01-03, under 510(k) number K854947.

Who is the listed applicant for REHABILITATION TABLES?

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

What is the FDA product code for REHABILITATION TABLES?

The FDA product code for REHABILITATION TABLES 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

Other records listing I-Rep, 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.

K930692LATHAM TABLEK930691ACCUTRAC TRACTION UNITK861864MEDTRON TYPE P-300 ULTRASONIC THERAPY UNITK851690ADJUSTABLE TREATMENT TABLESK842268VACUPULSE VACUUM UNITK832940ROTAGYM

View all 8 devices →

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.

↑