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FDA 510(k)

PULMO-PATTY

K-Number: K882604 · 1989-01-04

ApplicantTower Stopper, Inc.
Decision Date1989-01-04
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PULMO-PATTY is the device name listed in this FDA 510(k) record. The listed applicant is Tower Stopper, Inc.. It received FDA 510(k) clearance on 1989-01-04 under 510(k) number K882604. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULMO-PATTY?

PULMO-PATTY is a medical device that received FDA 510(k) clearance on 1989-01-04. The listed applicant is Tower Stopper, Inc.. The 510(k) number is K882604.

When did PULMO-PATTY receive FDA 510(k) clearance?

PULMO-PATTY received FDA 510(k) clearance on 1989-01-04, under 510(k) number K882604.

Who is the listed applicant for PULMO-PATTY?

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

What is the FDA product code for PULMO-PATTY?

The FDA product code for PULMO-PATTY is BYI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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