PORTA-POLE TM MEDICAL EQUIPMENT POLE W/FOLD
K-Number: K854082 · 1985-11-01
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Device Summary
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
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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