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FDA 510(k)

I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)

K-Number: K760263 · 1976-08-04

ApplicantForegger
Decision Date1976-08-04
Product CodeCBO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT) is the device name listed in this FDA 510(k) record. The listed applicant is Foregger. It received FDA 510(k) clearance on 1976-08-04 under 510(k) number K760263. The device is classified under product code CBO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)?

I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT) is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is Foregger. The 510(k) number is K760263.

When did I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT) receive FDA 510(k) clearance?

I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT) received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760263.

Who is the listed applicant for I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)?

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

What is the FDA product code for I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)?

The FDA product code for I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT) is CBO.

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 Foregger 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.

K771057ANESTHESIA MACHINE

Related Devices (Code: CBO)

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.

K811991SIMVACThe Lynn Terrell Co.K811908IMV MANIFOLDSAirlife, Inc.K791904IMV W/BAG & HOSES #M-509Mem Medical, Inc.K791912IMV FOR MONITORING #M-510Mem Medical, Inc.K791909IMV BUSHING #M-513Mem Medical, Inc.K791913IMV MANIFOLD #M-506Mem Medical, 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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