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FDA 510(k)

SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER

K-Number: K992986 · 1999-09-24

ApplicantSalter Labs
Decision Date1999-09-24
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Salter Labs. It received FDA 510(k) clearance on 1999-09-24 under 510(k) number K992986. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER?

SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER is a medical device that received FDA 510(k) clearance on 1999-09-24. The listed applicant is Salter Labs. The 510(k) number is K992986.

When did SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER receive FDA 510(k) clearance?

SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER received FDA 510(k) clearance on 1999-09-24, under 510(k) number K992986.

Who is the listed applicant for SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER?

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

What is the FDA product code for SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER?

The FDA product code for SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER is CAF.

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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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