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FDA 510(k)

MASTERLAB PFT AND MASTERLAB BODY BOX

K-Number: K893420 · 1989-06-23

ApplicantQuinton, Inc.
Decision Date1989-06-23
Product CodeCCM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASTERLAB PFT AND MASTERLAB BODY BOX is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K893420. The device is classified under product code CCM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTERLAB PFT AND MASTERLAB BODY BOX?

MASTERLAB PFT AND MASTERLAB BODY BOX is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Quinton, Inc.. The 510(k) number is K893420.

When did MASTERLAB PFT AND MASTERLAB BODY BOX receive FDA 510(k) clearance?

MASTERLAB PFT AND MASTERLAB BODY BOX received FDA 510(k) clearance on 1989-06-23, under 510(k) number K893420.

Who is the listed applicant for MASTERLAB PFT AND MASTERLAB BODY BOX?

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

What is the FDA product code for MASTERLAB PFT AND MASTERLAB BODY BOX?

The FDA product code for MASTERLAB PFT AND MASTERLAB BODY BOX is CCM.

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Related Devices (Code: CCM)

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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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