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FDA 510(k)

STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG

K-Number: K861056 · 1986-03-27

ApplicantIntertech/Ohio
Decision Date1986-03-27
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Intertech/Ohio. It received FDA 510(k) clearance on 1986-03-27 under 510(k) number K861056. 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 STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG?

STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG is a medical device that received FDA 510(k) clearance on 1986-03-27. The listed applicant is Intertech/Ohio. The 510(k) number is K861056.

When did STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG receive FDA 510(k) clearance?

STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG received FDA 510(k) clearance on 1986-03-27, under 510(k) number K861056.

Who is the listed applicant for STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG?

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

What is the FDA product code for STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG?

The FDA product code for STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG is BZA.

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Other records listing Intertech/Ohio 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.

K895144INTERTECH METERED DOSE ELBOWK890346INTERTECH UNIVERSAL HYDROPHOBIC FILTERK884525PEDIATRIC HUMIDIFIER TUBE W/ TEMPERATURE PORTK884526ADULT RESUSCITATOR WITH MASK AND FILTERK882204RESUSCITATOR VALVE ASSEMBLY W/FILTERK880394FIRST RESPONSE PEDIATRIC EMERGENCY RESUSCITATOR

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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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