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FDA 510(k)

KANGAROO NASOGASTRIC FEEDING TUBE

K-Number: K810854 · 1981-04-17

ApplicantChesebrough-Pond'S U.S.A. Co.
Decision Date1981-04-17
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KANGAROO NASOGASTRIC FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810854. 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 KANGAROO NASOGASTRIC FEEDING TUBE?

KANGAROO NASOGASTRIC FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K810854.

When did KANGAROO NASOGASTRIC FEEDING TUBE receive FDA 510(k) clearance?

KANGAROO NASOGASTRIC FEEDING TUBE received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810854.

Who is the listed applicant for KANGAROO NASOGASTRIC FEEDING TUBE?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KANGAROO NASOGASTRIC FEEDING TUBE?

The FDA product code for KANGAROO NASOGASTRIC FEEDING TUBE is KNT.

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Other records listing Chesebrough-Pond'S U.S.A. Co. 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.

K863866RESPIRADYNE II(TM)K862803CHESEBROUGH POND'S HYDROCOLLOID DRESSINGK851383BLISTERFILM TRANSPARENT DRESSINGK851382CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSINGK851539CHESEBROUGH-PONDS KANGAROO PUMP SET W/EASY-CAP CLOK843567KANGAROO NASOGASTRIC FEEDING TUBE

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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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