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FDA 510(k)

SUCTION TIPS

K-Number: K841159 · 1984-03-19

ApplicantMorwel Corp.
Decision Date1984-03-19
Product Code
DecisionUnknown

Device Summary

SUCTION TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Morwel Corp.. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K841159. FDA Decision: Unknown.

Frequently Asked Questions

What is the SUCTION TIPS?

SUCTION TIPS is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Morwel Corp.. The 510(k) number is K841159.

When did SUCTION TIPS receive FDA 510(k) clearance?

SUCTION TIPS received FDA 510(k) clearance on 1984-03-19, under 510(k) number K841159.

Who is the listed applicant for SUCTION TIPS?

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

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 Morwel 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.

K962525ULTRA-SAFE ULTRASONIC ASPIRATOR SYSTEMK841160MORWEL ASPIRATORK831520MORWEL CANNULA

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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