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FDA 510(k)

ENTERNAL Y EXTENSION SET RECORDER

K-Number: K840656 · 1984-04-04

ApplicantCorpak Medsystems
Decision Date1984-04-04
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERNAL Y EXTENSION SET RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Corpak Medsystems. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K840656. 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 ENTERNAL Y EXTENSION SET RECORDER?

ENTERNAL Y EXTENSION SET RECORDER is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Corpak Medsystems. The 510(k) number is K840656.

When did ENTERNAL Y EXTENSION SET RECORDER receive FDA 510(k) clearance?

ENTERNAL Y EXTENSION SET RECORDER received FDA 510(k) clearance on 1984-04-04, under 510(k) number K840656.

Who is the listed applicant for ENTERNAL Y EXTENSION SET RECORDER?

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 ENTERNAL Y EXTENSION SET RECORDER?

The FDA product code for ENTERNAL Y EXTENSION SET RECORDER 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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