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FDA 510(k)

MODIFIED JACKSON-REES CIRCUIT

K-Number: K790214 · 1979-03-19

ApplicantVital Signs, Inc.
Decision Date1979-03-19
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED JACKSON-REES CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1979-03-19 under 510(k) number K790214. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED JACKSON-REES CIRCUIT?

MODIFIED JACKSON-REES CIRCUIT is a medical device that received FDA 510(k) clearance on 1979-03-19. The listed applicant is Vital Signs, Inc.. The 510(k) number is K790214.

When did MODIFIED JACKSON-REES CIRCUIT receive FDA 510(k) clearance?

MODIFIED JACKSON-REES CIRCUIT received FDA 510(k) clearance on 1979-03-19, under 510(k) number K790214.

Who is the listed applicant for MODIFIED JACKSON-REES CIRCUIT?

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

What is the FDA product code for MODIFIED JACKSON-REES CIRCUIT?

The FDA product code for MODIFIED JACKSON-REES CIRCUIT is CAI.

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Related Devices (Code: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, 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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