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FDA 510(k)

PLASTIC TUBE EXTENTION SET

K-Number: K851047 · 1985-04-25

ApplicantMedovations, Inc.
Decision Date1985-04-25
Product Code
DecisionSubstantially Equivalent

Device Summary

PLASTIC TUBE EXTENTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Medovations, Inc.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K851047. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC TUBE EXTENTION SET?

PLASTIC TUBE EXTENTION SET is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Medovations, Inc.. The 510(k) number is K851047.

When did PLASTIC TUBE EXTENTION SET receive FDA 510(k) clearance?

PLASTIC TUBE EXTENTION SET received FDA 510(k) clearance on 1985-04-25, under 510(k) number K851047.

Who is the listed applicant for PLASTIC TUBE EXTENTION SET?

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

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Other records listing Medovations, Inc. 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.

K002363MEDOVATIONS ESOPHAGEAL DILATORK972119MALONEY BOUGE (1210-XX)/HURST BOUGIE (1212-XX)K924646OVER THE GUIDEWIRE DILATATION SYSTEMK913678TROCAR CATHETERK905478YANKAUER SUCTION DEVICEK874309URETHAL CATHETER

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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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