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FDA 510(k)

P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY

K-Number: K900884 · 1990-07-02

ApplicantApplied Medical Technologies
Decision Date1990-07-02
Product CodeKGC
Advisory CommitteeGU
DecisionUnknown

Device Summary

P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technologies. It received FDA 510(k) clearance on 1990-07-02 under 510(k) number K900884. 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 P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY?

P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY is a medical device that received FDA 510(k) clearance on 1990-07-02. The listed applicant is Applied Medical Technologies. The 510(k) number is K900884.

When did P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY receive FDA 510(k) clearance?

P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY received FDA 510(k) clearance on 1990-07-02, under 510(k) number K900884.

Who is the listed applicant for P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY?

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

What is the FDA product code for P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY?

The FDA product code for P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY is KGC.

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Other records listing Applied Medical Technologies 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.

K971434A.M.T. G-TUBE BALLOON REPLACEMENT GASTROSTOMY FEEDING DEVICEK972478PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIESK973893AMT BALLOON STOMA MEASURING DEVICES, AMT BALLOON MEASURING DEVICE, AMT BALLOON MEASURING DEVICE WITH STOP VALVE, AMY BAEK971757LOW PROFILE FEEDING SET ACCESSORYK971758CAUTERIZATION SMOKE EVACUATORK961345DOMED PERCUTANEOUS ENDOSCOPIC GASTROSTOMY(P.E.G.) FEEDING TUBE

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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.

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