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FDA 510(k)

NELSON-JUNG PLEURAL CATH

K-Number: K854812 · 1986-02-11

ApplicantResearch Medical, Inc.
Decision Date1986-02-11
Product CodeGBW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NELSON-JUNG PLEURAL CATH is the device name listed in this FDA 510(k) record. The listed applicant is Research Medical, Inc.. It received FDA 510(k) clearance on 1986-02-11 under 510(k) number K854812. The device is classified under product code GBW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NELSON-JUNG PLEURAL CATH?

NELSON-JUNG PLEURAL CATH is a medical device that received FDA 510(k) clearance on 1986-02-11. The listed applicant is Research Medical, Inc.. The 510(k) number is K854812.

When did NELSON-JUNG PLEURAL CATH receive FDA 510(k) clearance?

NELSON-JUNG PLEURAL CATH received FDA 510(k) clearance on 1986-02-11, under 510(k) number K854812.

Who is the listed applicant for NELSON-JUNG PLEURAL CATH?

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

What is the FDA product code for NELSON-JUNG PLEURAL CATH?

The FDA product code for NELSON-JUNG PLEURAL CATH is GBW.

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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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