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FDA 510(k)

NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC.

K-Number: K851981 · 1985-06-18

ApplicantSuperior Plastic Products Corp.
Decision Date1985-06-18
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC. 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 1985-06-18 under 510(k) number K851981. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC.?

NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC. is a medical device that received FDA 510(k) clearance on 1985-06-18. The listed applicant is Superior Plastic Products Corp.. The 510(k) number is K851981.

When did NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC. receive FDA 510(k) clearance?

NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC. received FDA 510(k) clearance on 1985-06-18, under 510(k) number K851981.

Who is the listed applicant for NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC.?

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 NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC.?

The FDA product code for NO. 5300-3 1/2 FRENCH UMBILICAL VESSEL CATH. ETC. is FOZ.

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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.

K8439759 FRENCH 42LONG POLYURETHANE GRADUATED ENTERIC FEK841945ENTERAL FEEDING BOTTLEK841630ENTERAL NUTRITION PUMPK840324SILICONE SUMP DRAIN 20 & 40 FRENCHK840323SILICONE SUCTION & IRRIGATION DRAINK841480INFECTION CONTROL VALVE

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Related Devices (Code: FOZ)

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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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