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FDA 510(k)

MICRO DIAMOND-POINT DISSECTION NEEDLES

K-Number: K962544 · 1996-09-20

ApplicantDsp Worldwide
Decision Date1996-09-20
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO DIAMOND-POINT DISSECTION NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Dsp Worldwide. It received FDA 510(k) clearance on 1996-09-20 under 510(k) number K962544. The device is classified under product code JOS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO DIAMOND-POINT DISSECTION NEEDLES?

MICRO DIAMOND-POINT DISSECTION NEEDLES is a medical device that received FDA 510(k) clearance on 1996-09-20. The listed applicant is Dsp Worldwide. The 510(k) number is K962544.

When did MICRO DIAMOND-POINT DISSECTION NEEDLES receive FDA 510(k) clearance?

MICRO DIAMOND-POINT DISSECTION NEEDLES received FDA 510(k) clearance on 1996-09-20, under 510(k) number K962544.

Who is the listed applicant for MICRO DIAMOND-POINT DISSECTION NEEDLES?

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

What is the FDA product code for MICRO DIAMOND-POINT DISSECTION NEEDLES?

The FDA product code for MICRO DIAMOND-POINT DISSECTION NEEDLES is JOS.

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 Dsp Worldwide 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.

K962371DERMTOME BLADEK962365XENON LIGHTSOURCE

Related Devices (Code: JOS)

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.

K161600Resection ElectrodesOlympus Winter & Ibe GmbHK050923LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATORConmed LinvatecK012684REPROCESSED ELECTROSURGICAL ELECTRODESterilmed, Inc.K011515MEDLINE GROUNDING PADMedline Industries, Inc.K003403ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999Highland / Marietta, Inc.K000333STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MODTriad Surgical Technologies, 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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