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)

PATIENT PAL I.V. WALKER

K-Number: K820963 · 1982-04-21

ApplicantPryor Products
Decision Date1982-04-21
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT PAL I.V. WALKER is the device name listed in this FDA 510(k) record. The listed applicant is Pryor Products. It received FDA 510(k) clearance on 1982-04-21 under 510(k) number K820963. The device is classified under product code FOX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT PAL I.V. WALKER?

PATIENT PAL I.V. WALKER is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Pryor Products. The 510(k) number is K820963.

When did PATIENT PAL I.V. WALKER receive FDA 510(k) clearance?

PATIENT PAL I.V. WALKER received FDA 510(k) clearance on 1982-04-21, under 510(k) number K820963.

Who is the listed applicant for PATIENT PAL I.V. WALKER?

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

What is the FDA product code for PATIENT PAL I.V. WALKER?

The FDA product code for PATIENT PAL I.V. WALKER is FOX.

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 Pryor Products 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.

K820964WHEELCHAIR PAL

Related Devices (Code: FOX)

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.

K980336IV STANDSClinton Industries, Inc.K964782MEDRAD CONTRAST HOLDERMedrad, Inc.K961470PORT-A-POLEPrins Medical Ind., Inc.K960027HIGH VOLUME I.V. & IRRIGATION TOWERAllen Medical Systems, Inc.K952196IV POLE/STANDValentine Intl. , Ltd.K950367IV SHUTTLEEquipment Concepts, 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.

↑