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FDA 510(k)

JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200

K-Number: K982136 · 1999-03-24

ApplicantSchiff & Co.
Decision Date1999-03-24
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 is the device name listed in this FDA 510(k) record. The listed applicant is Schiff & Co.. It received FDA 510(k) clearance on 1999-03-24 under 510(k) number K982136. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200?

JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 is a medical device that received FDA 510(k) clearance on 1999-03-24. The listed applicant is Schiff & Co.. The 510(k) number is K982136.

When did JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 receive FDA 510(k) clearance?

JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 received FDA 510(k) clearance on 1999-03-24, under 510(k) number K982136.

Who is the listed applicant for JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200?

The FDA 510(k) record lists Schiff & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200?

The FDA product code for JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 is DTN.

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Related Devices (Code: DTN)

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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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