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FDA 510(k)

ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7

K-Number: K854612 · 1986-01-03

ApplicantMed-West, Inc.
Decision Date1986-01-03
Product CodeLFK
Advisory CommitteeGU
DecisionUnknown

Device Summary

ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 is the device name listed in this FDA 510(k) record. The listed applicant is Med-West, Inc.. It received FDA 510(k) clearance on 1986-01-03 under 510(k) number K854612. The device is classified under product code LFK. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7?

ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 is a medical device that received FDA 510(k) clearance on 1986-01-03. The listed applicant is Med-West, Inc.. The 510(k) number is K854612.

When did ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 receive FDA 510(k) clearance?

ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 received FDA 510(k) clearance on 1986-01-03, under 510(k) number K854612.

Who is the listed applicant for ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7?

The FDA 510(k) record lists Med-West, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7?

The FDA product code for ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 is LFK.

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Related Devices (Code: LFK)

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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)Medron, Inc.K914936CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SETAkcess Medical Products, Inc.K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSAkcess Medical Products, Inc.K891763FC-100 FEMORAL CATHETERAkcess Medical Products, Inc.K891764FC-101 FEMORAL CATHETER GUIDE WIREAkcess Medical Products, Inc.K890717MODIFICATION HEMOFILTRATION CATHETER HF-100Vas-Cath, 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.

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