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FDA 510(k)

BUSH NECK W/TAP

K-Number: K841410 · 1984-04-18

ApplicantWarne Surgical Products, Ltd.
Decision Date1984-04-18
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BUSH NECK W/TAP is the device name listed in this FDA 510(k) record. The listed applicant is Warne Surgical Products, Ltd.. It received FDA 510(k) clearance on 1984-04-18 under 510(k) number K841410. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUSH NECK W/TAP?

BUSH NECK W/TAP is a medical device that received FDA 510(k) clearance on 1984-04-18. The listed applicant is Warne Surgical Products, Ltd.. The 510(k) number is K841410.

When did BUSH NECK W/TAP receive FDA 510(k) clearance?

BUSH NECK W/TAP received FDA 510(k) clearance on 1984-04-18, under 510(k) number K841410.

Who is the listed applicant for BUSH NECK W/TAP?

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

What is the FDA product code for BUSH NECK W/TAP?

The FDA product code for BUSH NECK W/TAP is DRM.

Other records listing Warne Surgical Products, Ltd. 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.

K850694WSP CODE 4310 STRESSCATHK850696WSP CODE 4300 DIOMASTER DIAGNOSTICK850695WSP CODE 4301 DIOMASTER THERAPEUTICK850693WSP CODE 4315 PADTESTK841511HAEMATURIA CATHETERSK840687KIDNEY TRANSPLANT CATHETER

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Related Devices (Code: DRM)

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.

K221700AutoPulse NXT Resuscitation SystemZoll Circulation, Inc.K211289RMU-2000 Automated Chest Compression SystemDefibtech, LLCK173553LUCAS 3 Chest Compression SystemJolife ABK161768LUCAS 3 Chest Compression SystemJolife ABK153628ROSC-U Mini Chest Compressor (RMCC)Resuscitation International, LLCK112998AUTOPULSE RESUSCITATION SYSTEM MODEL 1000Zoll Circulation

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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