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FDA 510(k)

BEAVER MICRO-GEM GAUGE BLOCK

K-Number: K860305 · 1986-02-12

ApplicantRudolph Beaver, Inc.
Decision Date1986-02-12
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BEAVER MICRO-GEM GAUGE BLOCK 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 1986-02-12 under 510(k) number K860305. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAVER MICRO-GEM GAUGE BLOCK?

BEAVER MICRO-GEM GAUGE BLOCK is a medical device that received FDA 510(k) clearance on 1986-02-12. The listed applicant is Rudolph Beaver, Inc.. The 510(k) number is K860305.

When did BEAVER MICRO-GEM GAUGE BLOCK receive FDA 510(k) clearance?

BEAVER MICRO-GEM GAUGE BLOCK received FDA 510(k) clearance on 1986-02-12, under 510(k) number K860305.

Who is the listed applicant for BEAVER MICRO-GEM GAUGE BLOCK?

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 MICRO-GEM GAUGE BLOCK?

The FDA product code for BEAVER MICRO-GEM GAUGE BLOCK 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 CYSTITOMEK852828BEAVER R-K KNIFEK853129BEAVER 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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