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FDA 510(k)

DINAMAP SELECT MULTI-PARAMETER SYSTEM

K-Number: K955113 · 1996-08-15

ApplicantJohnson & Johnson Medical, Inc.
Decision Date1996-08-15
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DINAMAP SELECT MULTI-PARAMETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 1996-08-15 under 510(k) number K955113. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DINAMAP SELECT MULTI-PARAMETER SYSTEM?

DINAMAP SELECT MULTI-PARAMETER SYSTEM is a medical device that received FDA 510(k) clearance on 1996-08-15. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K955113.

When did DINAMAP SELECT MULTI-PARAMETER SYSTEM receive FDA 510(k) clearance?

DINAMAP SELECT MULTI-PARAMETER SYSTEM received FDA 510(k) clearance on 1996-08-15, under 510(k) number K955113.

Who is the listed applicant for DINAMAP SELECT MULTI-PARAMETER SYSTEM?

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

What is the FDA product code for DINAMAP SELECT MULTI-PARAMETER SYSTEM?

The FDA product code for DINAMAP SELECT MULTI-PARAMETER SYSTEM is DPS.

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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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