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FDA 510(k)

TEMP-CHECK ADAPTOR, Y-CONFIGURATION

K-Number: K830921 · 1983-05-02

ApplicantCygnus Research Corp.
Decision Date1983-05-02
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TEMP-CHECK ADAPTOR, Y-CONFIGURATION is the device name listed in this FDA 510(k) record. The listed applicant is Cygnus Research Corp.. It received FDA 510(k) clearance on 1983-05-02 under 510(k) number K830921. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP-CHECK ADAPTOR, Y-CONFIGURATION?

TEMP-CHECK ADAPTOR, Y-CONFIGURATION is a medical device that received FDA 510(k) clearance on 1983-05-02. The listed applicant is Cygnus Research Corp.. The 510(k) number is K830921.

When did TEMP-CHECK ADAPTOR, Y-CONFIGURATION receive FDA 510(k) clearance?

TEMP-CHECK ADAPTOR, Y-CONFIGURATION received FDA 510(k) clearance on 1983-05-02, under 510(k) number K830921.

Who is the listed applicant for TEMP-CHECK ADAPTOR, Y-CONFIGURATION?

The FDA 510(k) record lists Cygnus Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMP-CHECK ADAPTOR, Y-CONFIGURATION?

The FDA product code for TEMP-CHECK ADAPTOR, Y-CONFIGURATION is BZO.

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 Cygnus Research Corp. 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.

K831556VAPOR-PHASE HUMIDIFIER SYSTEMK831163LO-COMP RESERVOIR-RE-1000K830923TEMP-CHECK ADAPTOR, STRAIGHT CONFIGURAK830922TEMP-CHECK ADAPTOR, TEE-CONFIGURATION

Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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