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FDA 510(k)

NEOTECH UNIVERSAL ADAPTER

K-Number: K882203 · 1988-06-17

ApplicantNeotech Products, Inc.
Decision Date1988-06-17
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEOTECH UNIVERSAL ADAPTER 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 1988-06-17 under 510(k) number K882203. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOTECH UNIVERSAL ADAPTER?

NEOTECH UNIVERSAL ADAPTER is a medical device that received FDA 510(k) clearance on 1988-06-17. The listed applicant is Neotech Products, Inc.. The 510(k) number is K882203.

When did NEOTECH UNIVERSAL ADAPTER receive FDA 510(k) clearance?

NEOTECH UNIVERSAL ADAPTER received FDA 510(k) clearance on 1988-06-17, under 510(k) number K882203.

Who is the listed applicant for NEOTECH UNIVERSAL ADAPTER?

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 UNIVERSAL ADAPTER?

The FDA product code for NEOTECH UNIVERSAL ADAPTER is BZA.

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 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 BAGK890425NEOTECH MUCUS TRAP W/CATHETERK880487NEOTECH MECONIUM ASPIRATOR (STERILE)

Related Devices (Code: BZA)

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.

K083702TRACH-ASSISTMergenet MedicalK954383SURELOC CIRCUIT CONNECTORPolamedco, Inc.K954197DISPOSABLE FLEX TUBEEngstrom MedicalK953786UNICOR, INC. CONNECTORS & AIRWAY EXTENSIONSUnicor, Inc.K952824NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTORIntertex Medical, Inc.K951345DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLINGCatheter Research, 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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