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FDA 510(k)

TU SUCTIONTRAP

K-Number: K884944 · 1989-02-03

ApplicantTulan Corp. C/O Richard Hamer Assoc.
Decision Date1989-02-03
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TU SUCTIONTRAP is the device name listed in this FDA 510(k) record. The listed applicant is Tulan Corp. C/O Richard Hamer Assoc.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K884944. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TU SUCTIONTRAP?

TU SUCTIONTRAP is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Tulan Corp. C/O Richard Hamer Assoc.. The 510(k) number is K884944.

When did TU SUCTIONTRAP receive FDA 510(k) clearance?

TU SUCTIONTRAP received FDA 510(k) clearance on 1989-02-03, under 510(k) number K884944.

Who is the listed applicant for TU SUCTIONTRAP?

The FDA 510(k) record lists Tulan Corp. C/O Richard Hamer Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TU SUCTIONTRAP?

The FDA product code for TU SUCTIONTRAP is BSY.

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 Tulan Corp. C/O Richard Hamer Assoc. 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.

K881805TU STOPCOCK

Related Devices (Code: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., 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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