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FDA 510(k)

SUCTION CATHETER STRAIGHT/COUDE

K-Number: K896730 · 1990-03-30

ApplicantUnoplast A/S
Decision Date1990-03-30
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SUCTION CATHETER STRAIGHT/COUDE is the device name listed in this FDA 510(k) record. The listed applicant is Unoplast A/S. It received FDA 510(k) clearance on 1990-03-30 under 510(k) number K896730. 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 SUCTION CATHETER STRAIGHT/COUDE?

SUCTION CATHETER STRAIGHT/COUDE is a medical device that received FDA 510(k) clearance on 1990-03-30. The listed applicant is Unoplast A/S. The 510(k) number is K896730.

When did SUCTION CATHETER STRAIGHT/COUDE receive FDA 510(k) clearance?

SUCTION CATHETER STRAIGHT/COUDE received FDA 510(k) clearance on 1990-03-30, under 510(k) number K896730.

Who is the listed applicant for SUCTION CATHETER STRAIGHT/COUDE?

The FDA 510(k) record lists Unoplast A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION CATHETER STRAIGHT/COUDE?

The FDA product code for SUCTION CATHETER STRAIGHT/COUDE 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 Unoplast A/S 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.

K896734FEEDING TUBEK896729NELATON-, FEMALE - OR TIEMANN CATHETERK896732UNOMETER 500K896731OXYGEN CATHETERSK896733VACCONK802248DISARP ORIGINAL

View all 7 devices →

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

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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