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FDA 510(k)

PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD

K-Number: K854082 · 1985-11-01

Decision Date1985-11-01
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD is the device name listed in this FDA 510(k) record. The listed applicant is Gray Wave Corp.. It received FDA 510(k) clearance on 1985-11-01 under 510(k) number K854082. 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 PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD?

PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD is a medical device that received FDA 510(k) clearance on 1985-11-01. The listed applicant is Gray Wave Corp.. The 510(k) number is K854082.

When did PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD receive FDA 510(k) clearance?

PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD received FDA 510(k) clearance on 1985-11-01, under 510(k) number K854082.

Who is the listed applicant for PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD?

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

What is the FDA product code for PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD?

The FDA product code for PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD 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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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