Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GASTROSTOMY FEEDING CATHETER

K-Number: K901795 · 1990-08-08

ApplicantSouthside Biotechnology
Decision Date1990-08-08
Product CodeKGC
Advisory CommitteeGU
DecisionUnknown

Device Summary

GASTROSTOMY FEEDING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Southside Biotechnology. It received FDA 510(k) clearance on 1990-08-08 under 510(k) number K901795. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the GASTROSTOMY FEEDING CATHETER?

GASTROSTOMY FEEDING CATHETER is a medical device that received FDA 510(k) clearance on 1990-08-08. The listed applicant is Southside Biotechnology. The 510(k) number is K901795.

When did GASTROSTOMY FEEDING CATHETER receive FDA 510(k) clearance?

GASTROSTOMY FEEDING CATHETER received FDA 510(k) clearance on 1990-08-08, under 510(k) number K901795.

Who is the listed applicant for GASTROSTOMY FEEDING CATHETER?

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

What is the FDA product code for GASTROSTOMY FEEDING CATHETER?

The FDA product code for GASTROSTOMY FEEDING CATHETER is KGC.

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 Southside Biotechnology 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.

K901791PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH.K884439GASTROSTOMY FEEDING DEVICE

Related Devices (Code: KGC)

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.

K242211PUMA-G Pediatric SystemCoaptech, Inc.K223916PUMA-G SystemCoaptech, Inc.K193612AMT Suture Delivery SystemApplied Medical Technology, Inc.K191844Fidmi Low Profile Enteral Feeding DeviceFidmi Medical, Ltd.K182832Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor SetCook IncorporatedK183057PUMA-G SystemCoaptech, LLC

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.

↑