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FDA 510(k)

CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD)

K-Number: K990127 · 1999-02-10

ApplicantCorpak Medsystems
Decision Date1999-02-10
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD) is the device name listed in this FDA 510(k) record. The listed applicant is Corpak Medsystems. It received FDA 510(k) clearance on 1999-02-10 under 510(k) number K990127. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD)?

CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD) is a medical device that received FDA 510(k) clearance on 1999-02-10. The listed applicant is Corpak Medsystems. The 510(k) number is K990127.

When did CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD) receive FDA 510(k) clearance?

CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD) received FDA 510(k) clearance on 1999-02-10, under 510(k) number K990127.

Who is the listed applicant for CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD)?

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

What is the FDA product code for CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD)?

The FDA product code for CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD) is KNT.

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Other records listing Corpak Medsystems 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.

K131532ELECTROMAGNETIC TRANSMITTING STYLETK113351CORTRAK ENTERAL ACCESS DEVICEK100365FARRELL VALVE WITH CORFLO ANTI-IV CONNECTORS MODEL 20-4300AIVK091637CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900K083776CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1030AIV-LB-SK083791CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S

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Related Devices (Code: KNT)

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.

K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®Boehringer Laboratories, LLCK253514Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric Tube - 20 French (0092100); Blakemore Esophageal-Nasogastric Tube - 16 French (0092300)C.R. Bard, Inc.K250389XNY Disposable Gastric Calibration TubeChangzhou Xin Neng Yuan Medical Stapler Co.,LtdK243228Flexi-Seal AIR (with ENFit Connector)ConvatecK242336hygh-tec Drainage IIAmb MedtecK242901ZZIREN™ Orogastric Tube; ZZIREN™ SGT Orogastric Tube - 32 Fr (ZZ-SGT-32); ZZIREN™ SGT Orogastric Tube - 36 Fr (ZZ-SGT-36); ZZIREN™ SGT Orogastric Tube - 40 Fr (ZZ-SGT-40); ZZIREN™ GBT Orogastric Tube - 32 Fr (ZZ-GBT-32); ZZIREN™ GBT Orogastric Tube - 36 Fr (ZZ-GBT-36); ZZIREN™ GBT Orogastric Tube - 40 Fr (ZZ-GBT-40)Tools For Surgery, 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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