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FDA 510(k)

ENTERAL FEEDING BOTTLE

K-Number: K841945 · 1984-07-26

ApplicantSuperior Plastic Products Corp.
Decision Date1984-07-26
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL FEEDING BOTTLE is the device name listed in this FDA 510(k) record. The listed applicant is Superior Plastic Products Corp.. It received FDA 510(k) clearance on 1984-07-26 under 510(k) number K841945. 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 ENTERAL FEEDING BOTTLE?

ENTERAL FEEDING BOTTLE is a medical device that received FDA 510(k) clearance on 1984-07-26. The listed applicant is Superior Plastic Products Corp.. The 510(k) number is K841945.

When did ENTERAL FEEDING BOTTLE receive FDA 510(k) clearance?

ENTERAL FEEDING BOTTLE received FDA 510(k) clearance on 1984-07-26, under 510(k) number K841945.

Who is the listed applicant for ENTERAL FEEDING BOTTLE?

The FDA 510(k) record lists Superior Plastic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENTERAL FEEDING BOTTLE?

The FDA product code for ENTERAL FEEDING BOTTLE is KNT.

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Other records listing Superior Plastic Products Corp. 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.

K851981NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC.K8439759 FRENCH 42LONG POLYURETHANE GRADUATED ENTERIC FEK841630ENTERAL NUTRITION PUMPK841480INFECTION CONTROL VALVEK840323SILICONE SUCTION & IRRIGATION DRAINK840324SILICONE SUMP DRAIN 20 & 40 FRENCH

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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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