FDA 510(k)

SAMSON 1000 ANESTHESIA CIRCUIT

K-Number: K842488 · 1984-07-06

Decision Date1984-07-06

Product CodeCAI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SAMSON 1000 ANESTHESIA CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is J. H. Emerson Co.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K842488. 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 SAMSON 1000 ANESTHESIA CIRCUIT?

SAMSON 1000 ANESTHESIA CIRCUIT is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is J. H. Emerson Co.. The 510(k) number is K842488.

When did SAMSON 1000 ANESTHESIA CIRCUIT receive FDA 510(k) clearance?

SAMSON 1000 ANESTHESIA CIRCUIT received FDA 510(k) clearance on 1984-07-06, under 510(k) number K842488.

Who is the listed applicant for SAMSON 1000 ANESTHESIA CIRCUIT?

The FDA 510(k) record lists J. H. Emerson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAMSON 1000 ANESTHESIA CIRCUIT?

The FDA product code for SAMSON 1000 ANESTHESIA CIRCUIT is CAI.

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Other records listing J. H. Emerson Co. as applicant

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Related Devices (Code: CAI)

K954480CONDENSATE COLLECTION KITNova-Ventrx K953787UNICOR, 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.