Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CUTTER POINTS

K-Number: K792250 · 1980-01-23

ApplicantCutter Laboratories, Inc.
Decision Date1980-01-23
Product CodeEHL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CUTTER POINTS is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1980-01-23 under 510(k) number K792250. The device is classified under product code EHL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTTER POINTS?

CUTTER POINTS is a medical device that received FDA 510(k) clearance on 1980-01-23. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K792250.

When did CUTTER POINTS receive FDA 510(k) clearance?

CUTTER POINTS received FDA 510(k) clearance on 1980-01-23, under 510(k) number K792250.

Who is the listed applicant for CUTTER POINTS?

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

What is the FDA product code for CUTTER POINTS?

The FDA product code for CUTTER POINTS is EHL.

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 Cutter Laboratories, 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.

K861315HYPERBARIC PENETRATION EXTENSION SETK854106BAYSILEXK842324PERFOURMK834106INTRAVENOUS INFUSION CONTROLLERK832237ORTHOPEDIC CASTING TAPE MAXCASTK823214DOSIMETRIC RELEASE PROGRAM - ADMIN. SET

View all 39 devices →

Related Devices (Code: EHL)

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.

K780811DENTAL ABRASIVE DEVICECavitron Corp.K780376MINIDENTOFLEX NEW POLISHING SYSTEMCavitron Corp.K780377PINIDENTOFLEX DENTAL POLISHERCavitron Corp.

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.

↑