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FDA 510(k)

MOSSMED DUAL INTERMITTENT ASPIRATOR

K-Number: K031492 · 2004-02-05

ApplicantMoss Medical Products
Decision Date2004-02-05
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOSSMED DUAL INTERMITTENT ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Moss Medical Products. It received FDA 510(k) clearance on 2004-02-05 under 510(k) number K031492. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOSSMED DUAL INTERMITTENT ASPIRATOR?

MOSSMED DUAL INTERMITTENT ASPIRATOR is a medical device that received FDA 510(k) clearance on 2004-02-05. The listed applicant is Moss Medical Products. The 510(k) number is K031492.

When did MOSSMED DUAL INTERMITTENT ASPIRATOR receive FDA 510(k) clearance?

MOSSMED DUAL INTERMITTENT ASPIRATOR received FDA 510(k) clearance on 2004-02-05, under 510(k) number K031492.

Who is the listed applicant for MOSSMED DUAL INTERMITTENT ASPIRATOR?

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

What is the FDA product code for MOSSMED DUAL INTERMITTENT ASPIRATOR?

The FDA product code for MOSSMED DUAL INTERMITTENT ASPIRATOR is KNT.

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Other records listing Moss Medical Products 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.

K051206Y2K2 ENTERNAL TUBE FLUID FILTERK030413Y2K2 ENTERNAL FEEDING MANAGERK913701MOSS - ANCHOR SETK910910MOSS- ANCHOR SETK910912MOSS NASAL TUBE MARK IVK910911MOSS P.E.G. TRAY

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Related Devices (Code: KNT)

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.

K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®Boehringer Laboratories, LLCK253514Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric Tube - 20 French (0092100); Blakemore Esophageal-Nasogastric Tube - 16 French (0092300)C.R. Bard, Inc.K250389XNY Disposable Gastric Calibration TubeChangzhou Xin Neng Yuan Medical Stapler Co.,LtdK243228Flexi-Seal AIR (with ENFit Connector)ConvatecK242336hygh-tec Drainage IIAmb MedtecK242901ZZIREN™ Orogastric Tube; ZZIREN™ SGT Orogastric Tube - 32 Fr (ZZ-SGT-32); ZZIREN™ SGT Orogastric Tube - 36 Fr (ZZ-SGT-36); ZZIREN™ SGT Orogastric Tube - 40 Fr (ZZ-SGT-40); ZZIREN™ GBT Orogastric Tube - 32 Fr (ZZ-GBT-32); ZZIREN™ GBT Orogastric Tube - 36 Fr (ZZ-GBT-36); ZZIREN™ GBT Orogastric Tube - 40 Fr (ZZ-GBT-40)Tools For Surgery, LLC

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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