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FDA 510(k)

VEINPREP VEIN GRAFT PREP. KIT A277723

K-Number: K830150 · 1983-02-28

ApplicantAtrium Medical Corp.
Decision Date1983-02-28
Product CodeDWD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VEINPREP VEIN GRAFT PREP. KIT A277723 is the device name listed in this FDA 510(k) record. The listed applicant is Atrium Medical Corp.. It received FDA 510(k) clearance on 1983-02-28 under 510(k) number K830150. The device is classified under product code DWD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEINPREP VEIN GRAFT PREP. KIT A277723?

VEINPREP VEIN GRAFT PREP. KIT A277723 is a medical device that received FDA 510(k) clearance on 1983-02-28. The listed applicant is Atrium Medical Corp.. The 510(k) number is K830150.

When did VEINPREP VEIN GRAFT PREP. KIT A277723 receive FDA 510(k) clearance?

VEINPREP VEIN GRAFT PREP. KIT A277723 received FDA 510(k) clearance on 1983-02-28, under 510(k) number K830150.

Who is the listed applicant for VEINPREP VEIN GRAFT PREP. KIT A277723?

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

What is the FDA product code for VEINPREP VEIN GRAFT PREP. KIT A277723?

The FDA product code for VEINPREP VEIN GRAFT PREP. KIT A277723 is DWD.

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Other records listing Atrium Medical 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.

K130131EDRAIN CHEST DRAINAGE SYSTEMK122138ATRIUM FLIXENE IFG VASCULAR GRAFTK121070C-QUR RPM MESHK113112CLEARWAY RX NB CATHETERK102596ATRIUM GRADUATED WALL FLIXENE AX-BIFEM GRAFTK093431CLEARWAY OTW MODEL 85912

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Related Devices (Code: DWD)

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.

K992657IBC VRV, MODEL 1350International Biophysics Corp.K920077NIKKISO NK PUMPInternational Medical Products, Inc.K915480B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.Bd Becton Dickinson Vacutainer Systems PreanalyticK915481B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINTBd Becton Dickinson Vacutainer Systems PreanalyticK915482B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PTBd Becton Dickinson Vacutainer Systems PreanalyticK905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.Baxter Bentley Laboratories, 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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