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FDA 510(k)

NEOTECH MUCUS TRAP W/CATHETER

K-Number: K890425 · 1989-04-19

ApplicantNeotech Products, Inc.
Decision Date1989-04-19
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEOTECH MUCUS TRAP W/CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Neotech Products, Inc.. It received FDA 510(k) clearance on 1989-04-19 under 510(k) number K890425. 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 NEOTECH MUCUS TRAP W/CATHETER?

NEOTECH MUCUS TRAP W/CATHETER is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is Neotech Products, Inc.. The 510(k) number is K890425.

When did NEOTECH MUCUS TRAP W/CATHETER receive FDA 510(k) clearance?

NEOTECH MUCUS TRAP W/CATHETER received FDA 510(k) clearance on 1989-04-19, under 510(k) number K890425.

Who is the listed applicant for NEOTECH MUCUS TRAP W/CATHETER?

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

What is the FDA product code for NEOTECH MUCUS TRAP W/CATHETER?

The FDA product code for NEOTECH MUCUS TRAP W/CATHETER is BSY.

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Other records listing Neotech Products, 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.

K011564NEOLEADK931727URINARY DRAINAGE BAG CADDYK921024URO-TOTE LEG BAGK882203NEOTECH UNIVERSAL ADAPTERK880487NEOTECH MECONIUM ASPIRATOR (STERILE)

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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