FDA 510(k)

NOSE CLIP

K-Number: K760461 · 1976-08-26

Decision Date1976-08-26

Product CodeBXJ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

NOSE CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1976-08-26 under 510(k) number K760461. The device is classified under product code BXJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOSE CLIP?

NOSE CLIP is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is Inspiron Corp.. The 510(k) number is K760461.

When did NOSE CLIP receive FDA 510(k) clearance?

NOSE CLIP received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760461.

Who is the listed applicant for NOSE CLIP?

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

What is the FDA product code for NOSE CLIP?

The FDA product code for NOSE CLIP is BXJ.

Other records listing Inspiron Corp. 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.

K860838INSPIRON DOUBLE SWIVEL TRACH ADAPTER K850346OXYGEN CONCENTRATOR K843932VAPOR-PHASE HUMIDIFIER SYS-ADVANCED K840935MANUAL RESUSCITATION SYSTEM K841158NEBULO 28 NEBULIZER KIT K840418INSPIRATORY/EXPIRATORY MUSCLE EXERCIS

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Related Devices (Code: BXJ)

K853578MEDIPART DISPOS. NOSE CLIP MP-2001Medipart Jerry Alexander K810339NOSECLIP #6118Todd Industries, Inc.K770015NOSECLIP FOR RESP. CARE & PULMON. FUNC.Bd Becton Dickinson Vacutainer Systems Preanalytic

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.