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FDA 510(k)

FLEX TUBE

K-Number: K881230 · 1988-04-14

ApplicantIntertech Resources, Inc.
Decision Date1988-04-14
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLEX TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1988-04-14 under 510(k) number K881230. 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 FLEX TUBE?

FLEX TUBE is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K881230.

When did FLEX TUBE receive FDA 510(k) clearance?

FLEX TUBE received FDA 510(k) clearance on 1988-04-14, under 510(k) number K881230.

Who is the listed applicant for FLEX TUBE?

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

What is the FDA product code for FLEX TUBE?

The FDA product code for FLEX TUBE is BZA.

Other records listing Intertech Resources, 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.

K9613181ST RESPONSE DISPOSABLE MANOMETERK955008HEAT & MOISTURE EXCHANGERK953580HEAT MOISTURE EXCHANGERK952223XENON GAS BREATHING CIRCUITK952062PFT FILTERK952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC

View all 29 devices →

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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