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FDA 510(k)

BEAVER R-K KNIFE

K-Number: K852828 · 1985-11-04

ApplicantRudolph Beaver, Inc.
Decision Date1985-11-04
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent for Some Indications

Device Summary

BEAVER R-K KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Rudolph Beaver, Inc.. It received FDA 510(k) clearance on 1985-11-04 under 510(k) number K852828. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BEAVER R-K KNIFE?

BEAVER R-K KNIFE is a medical device that received FDA 510(k) clearance on 1985-11-04. The listed applicant is Rudolph Beaver, Inc.. The 510(k) number is K852828.

When did BEAVER R-K KNIFE receive FDA 510(k) clearance?

BEAVER R-K KNIFE received FDA 510(k) clearance on 1985-11-04, under 510(k) number K852828.

Who is the listed applicant for BEAVER R-K KNIFE?

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

What is the FDA product code for BEAVER R-K KNIFE?

The FDA product code for BEAVER R-K KNIFE is HNN.

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 Rudolph Beaver, Inc. 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.

K883361ARTHRO-TRAC(TM)K875030OCU-1K862709MECHANICAL CYSTITOMEK860305BEAVER MICRO-GEM GAUGE BLOCKK853129BEAVER MULTIPURPOSE SAPPHIRE KNIFE

Related Devices (Code: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, 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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