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FDA 510(k)

MOISTAIR FLUID AIR TUBING SET

K-Number: K974561 · 1998-02-19

ApplicantAmerican Medical Devices, Inc.
Decision Date1998-02-19
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MOISTAIR FLUID AIR TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Devices, Inc.. It received FDA 510(k) clearance on 1998-02-19 under 510(k) number K974561. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOISTAIR FLUID AIR TUBING SET?

MOISTAIR FLUID AIR TUBING SET is a medical device that received FDA 510(k) clearance on 1998-02-19. The listed applicant is American Medical Devices, Inc.. The 510(k) number is K974561.

When did MOISTAIR FLUID AIR TUBING SET receive FDA 510(k) clearance?

MOISTAIR FLUID AIR TUBING SET received FDA 510(k) clearance on 1998-02-19, under 510(k) number K974561.

Who is the listed applicant for MOISTAIR FLUID AIR TUBING SET?

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

What is the FDA product code for MOISTAIR FLUID AIR TUBING SET?

The FDA product code for MOISTAIR FLUID AIR TUBING SET is KYG.

Related Clinical Trials

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Other records listing American Medical Devices, 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.

K971853ENDOVIEW SPPHIRE LENS SETK970882ENDOLIGHT END IRRIGATING ENDO-ILLUMINATOR (20 GA. AND 19 GA.)K970875ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.)K970873ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)K970878ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT

Related Devices (Code: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K971173ML DISPOSABLE ALK TUBINGMed-Logics, Inc.

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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