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FDA 510(k)

MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER

K-Number: K873423 · 1987-11-06

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1987-11-06
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K873423. 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 MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER?

MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K873423.

When did MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER receive FDA 510(k) clearance?

MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER received FDA 510(k) clearance on 1987-11-06, under 510(k) number K873423.

Who is the listed applicant for MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER?

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

What is the FDA product code for MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER?

The FDA product code for MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER is 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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