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FDA 510(k)

EPIDURAL CATHETER TRAY

K-Number: K840201 · 1984-03-02

ApplicantAries Medical, Inc.
Decision Date1984-03-02
Product CodeMJL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EPIDURAL CATHETER TRAY 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 1984-03-02 under 510(k) number K840201. The device is classified under product code MJL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPIDURAL CATHETER TRAY?

EPIDURAL CATHETER TRAY is a medical device that received FDA 510(k) clearance on 1984-03-02. The listed applicant is Aries Medical, Inc.. The 510(k) number is K840201.

When did EPIDURAL CATHETER TRAY receive FDA 510(k) clearance?

EPIDURAL CATHETER TRAY received FDA 510(k) clearance on 1984-03-02, under 510(k) number K840201.

Who is the listed applicant for EPIDURAL CATHETER TRAY?

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

What is the FDA product code for EPIDURAL CATHETER TRAY?

The FDA product code for EPIDURAL CATHETER TRAY is MJL.

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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

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Related Devices (Code: MJL)

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.

K923859PREMIER BLASTOMYCESMeridian Diagnostics, Inc.

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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