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FDA 510(k)

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH.

K-Number: K901791 · 1990-08-08

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

Device Summary

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH. 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 K901791. 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 PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH.?

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH. 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 K901791.

When did PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH. receive FDA 510(k) clearance?

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH. received FDA 510(k) clearance on 1990-08-08, under 510(k) number K901791.

Who is the listed applicant for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH.?

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 PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH.?

The FDA product code for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH. is KGC.

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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.

K901795GASTROSTOMY FEEDING CATHETERK884439GASTROSTOMY 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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