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FDA 510(k)

VESSEL DILATOR

K-Number: K840641 · 1984-02-14

ApplicantAries Medical, Inc.
Decision Date1984-02-14
Product Code
DecisionUnknown

Device Summary

VESSEL DILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Aries Medical, Inc.. It received FDA 510(k) clearance on 1984-02-14 under 510(k) number K840641. FDA Decision: Unknown.

Frequently Asked Questions

What is the VESSEL DILATOR?

VESSEL DILATOR is a medical device that received FDA 510(k) clearance on 1984-02-14. The listed applicant is Aries Medical, Inc.. The 510(k) number is K840641.

When did VESSEL DILATOR receive FDA 510(k) clearance?

VESSEL DILATOR received FDA 510(k) clearance on 1984-02-14, under 510(k) number K840641.

Who is the listed applicant for VESSEL DILATOR?

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

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Other records listing Aries Medical, 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.

K912604SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIFK903925ARIES MELDICAL MODEL 2100HC HANK CRANKK903442ARIES TAPERSEAL(TM) SHEATHK895433ARIES 30CC & 50CC INTRA-AORTIC BALLOON & CONT. SYSK882289ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH.K86499440CC PER. PRE-FURL (S/L) INTRA-AORTIC CATHETER

View all 19 devices →

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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