FDA 510(k)

OB HELP ARM

K-Number: K830842 · 1983-04-05

Decision Date1983-04-05

Product CodeILE

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

OB HELP ARM 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 K830842. The device is classified under product code ILE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OB HELP ARM?

OB HELP ARM 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 K830842.

When did OB HELP ARM receive FDA 510(k) clearance?

OB HELP ARM received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830842.

Who is the listed applicant for OB HELP ARM?

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 OB HELP ARM?

The FDA product code for OB HELP ARM is ILE.

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 TABLE K854730DAISY (ABSORBENT INCONTINENCE SHIELD)K854729ADAM (ABSORBENT INCONTINENCE SHIELD)K851471TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR K851470BIBAG, BIBAND & BIFIX - SINGLE USE URINE COLLECTOR

View all 17 devices →

Related Devices (Code: ILE)

K823811OVERHEAD ARM SLINGSDanek Medical, Inc.K823152OB HELP ARMOrthion Corp.

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.