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FDA 510(k)

NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR

K-Number: K894653 · 1989-12-21

ApplicantSuperior Biosystems, Inc.
Decision Date1989-12-21
Product CodeKGC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR is the device name listed in this FDA 510(k) record. The listed applicant is Superior Biosystems, Inc.. It received FDA 510(k) clearance on 1989-12-21 under 510(k) number K894653. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR?

NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR is a medical device that received FDA 510(k) clearance on 1989-12-21. The listed applicant is Superior Biosystems, Inc.. The 510(k) number is K894653.

When did NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR receive FDA 510(k) clearance?

NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR received FDA 510(k) clearance on 1989-12-21, under 510(k) number K894653.

Who is the listed applicant for NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR?

The FDA 510(k) record lists Superior Biosystems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR?

The FDA product code for NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR is KGC.

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Related Devices (Code: KGC)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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