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FDA 510(k)

SUCTION CANNULAS

K-Number: K841249 · 1984-06-04

ApplicantCustom Surgical Products, Inc.
Decision Date1984-06-04
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUCTION CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Custom Surgical Products, Inc.. It received FDA 510(k) clearance on 1984-06-04 under 510(k) number K841249. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION CANNULAS?

SUCTION CANNULAS is a medical device that received FDA 510(k) clearance on 1984-06-04. The listed applicant is Custom Surgical Products, Inc.. The 510(k) number is K841249.

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

SUCTION CANNULAS received FDA 510(k) clearance on 1984-06-04, under 510(k) number K841249.

Who is the listed applicant for SUCTION CANNULAS?

The FDA 510(k) record lists Custom Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION CANNULAS?

The FDA product code for SUCTION CANNULAS is GEA.

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 Custom Surgical Products, Inc. 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.

K870874CSPI SPECIMEN TRAP (NON-STERILE)K841383CSPI ROTARY SURGICAL ASPIRATORK841242CSPI PREMIUM SURGICAL ASPIRATOR

Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, 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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