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FDA 510(k)

NU-TRAP SUCTION CATHETER W/MUCUS TRAP

K-Number: K893462 · 1989-06-08

ApplicantAtheus Corp.
Decision Date1989-06-08
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NU-TRAP SUCTION CATHETER W/MUCUS TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Atheus Corp.. It received FDA 510(k) clearance on 1989-06-08 under 510(k) number K893462. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NU-TRAP SUCTION CATHETER W/MUCUS TRAP?

NU-TRAP SUCTION CATHETER W/MUCUS TRAP is a medical device that received FDA 510(k) clearance on 1989-06-08. The listed applicant is Atheus Corp.. The 510(k) number is K893462.

When did NU-TRAP SUCTION CATHETER W/MUCUS TRAP receive FDA 510(k) clearance?

NU-TRAP SUCTION CATHETER W/MUCUS TRAP received FDA 510(k) clearance on 1989-06-08, under 510(k) number K893462.

Who is the listed applicant for NU-TRAP SUCTION CATHETER W/MUCUS TRAP?

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

What is the FDA product code for NU-TRAP SUCTION CATHETER W/MUCUS TRAP?

The FDA product code for NU-TRAP SUCTION CATHETER W/MUCUS TRAP is BSY.

Related Clinical Trials

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.

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Other records listing Atheus Corp. 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.

K905606EXTERNAL FETAL MONITOR TRANSDUCER HOLDER

Related Devices (Code: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., 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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