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FDA 510(k)

RESI-WALKER

K-Number: K830848 · 1983-04-05

ApplicantLic-Orthion
Decision Date1983-04-05
Product CodeITJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RESI-WALKER is the device name listed in this FDA 510(k) record. The listed applicant is Lic-Orthion. It received FDA 510(k) clearance on 1983-04-05 under 510(k) number K830848. The device is classified under product code ITJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESI-WALKER?

RESI-WALKER is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is Lic-Orthion. The 510(k) number is K830848.

When did RESI-WALKER receive FDA 510(k) clearance?

RESI-WALKER received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830848.

Who is the listed applicant for RESI-WALKER?

The FDA 510(k) record lists Lic-Orthion as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESI-WALKER?

The FDA product code for RESI-WALKER is ITJ.

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Other records listing Lic-Orthion 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.

K891649PATIENT EXAMINATION GLOVES (LATEX)K862022LIC-ORTHION MULTI-THERAPY TREATMENT TABLEK854730DAISY (ABSORBENT INCONTINENCE SHIELD)K854729ADAM (ABSORBENT INCONTINENCE SHIELD)K851471TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTORK851470BIBAG, BIBAND & BIFIX - SINGLE USE URINE COLLECTOR

View all 17 devices →

Related Devices (Code: ITJ)

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.

K833869CHILD'S WALKERKaye Products, Inc.K833195UMBRELLA WALKERConvaid Products, Inc.K830784WALK N ROLLMeta-MorrisK823105RESI-WALKEROrthion Corp.K821404LIGHT WEIGHT ALUMINUM WALKERManuco Manufacturing Co., Inc.K820711WALK-A-CYCLEWalk-A-Cycle Division

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.

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