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FDA 510(k)

MODEL# 7500 SURVEYOR

K-Number: K944611 · 1995-04-21

ApplicantDevilbiss Health Care, Inc.
Decision Date1995-04-21
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL# 7500 SURVEYOR is the device name listed in this FDA 510(k) record. The listed applicant is Devilbiss Health Care, Inc.. It received FDA 510(k) clearance on 1995-04-21 under 510(k) number K944611. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL# 7500 SURVEYOR?

MODEL# 7500 SURVEYOR is a medical device that received FDA 510(k) clearance on 1995-04-21. The listed applicant is Devilbiss Health Care, Inc.. The 510(k) number is K944611.

When did MODEL# 7500 SURVEYOR receive FDA 510(k) clearance?

MODEL# 7500 SURVEYOR received FDA 510(k) clearance on 1995-04-21, under 510(k) number K944611.

Who is the listed applicant for MODEL# 7500 SURVEYOR?

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

What is the FDA product code for MODEL# 7500 SURVEYOR?

The FDA product code for MODEL# 7500 SURVEYOR is MNR.

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Other records listing Devilbiss Health Care, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K963349DEVILBISS 8650DK970289COMPRESSOR/NEBULIZER #3650K961126PULSE DOSE SERIESK950849MODEL #7354K952491MODEL 7355K952249JET NEBULIZER

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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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