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)

NIPPER, NAIL, P610 ENGLISH

K-Number: K770303 · 1977-03-09

ApplicantDentronix, Inc.
Decision Date1977-03-09
Product CodeFZT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NIPPER, NAIL, P610 ENGLISH is the device name listed in this FDA 510(k) record. The listed applicant is Dentronix, Inc.. It received FDA 510(k) clearance on 1977-03-09 under 510(k) number K770303. The device is classified under product code FZT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIPPER, NAIL, P610 ENGLISH?

NIPPER, NAIL, P610 ENGLISH is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Dentronix, Inc.. The 510(k) number is K770303.

When did NIPPER, NAIL, P610 ENGLISH receive FDA 510(k) clearance?

NIPPER, NAIL, P610 ENGLISH received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770303.

Who is the listed applicant for NIPPER, NAIL, P610 ENGLISH?

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

What is the FDA product code for NIPPER, NAIL, P610 ENGLISH?

The FDA product code for NIPPER, NAIL, P610 ENGLISH is FZT.

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 Dentronix, 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.

K910202DENTRONIX MODEL 2000K880322DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEMK771006MODIFIED PODIATRY PRODUCTSK771005NEW PODIATRY PRODUCTSK770302CUTTER, P606 BONEK770305CUTTER, P607 BONE

View all 9 devices →

Related Devices (Code: FZT)

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.

K112400SMARTSHEARSNuscience Consulting and Management Group, LLCK890818AUTO SUTURE DISPOSABLE SURGICAL TROCAR*United States Surgical, A Division of Tyco HealthcK872990MICRINS SURGICAL SCISSORMicrins Surgical, Inc.K841741SINGLE HAIR TRANSPLANT GRAFTParis Products, Inc.K841247SPC DISPOSABLE CUTTERSurgical Products Corp.K822448SCISSORS, VARIOUSJ. Sklar Mfg. Co., 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.

↑