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FDA 510(k)

HI-MID CURCUIT

K-Number: K771034 · 1977-08-04

ApplicantDraeger Medical, Inc.
Decision Date1977-08-04
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HI-MID CURCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical, Inc.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771034. 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 HI-MID CURCUIT?

HI-MID CURCUIT is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K771034.

When did HI-MID CURCUIT receive FDA 510(k) clearance?

HI-MID CURCUIT received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771034.

Who is the listed applicant for HI-MID CURCUIT?

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

What is the FDA product code for HI-MID CURCUIT?

The FDA product code for HI-MID CURCUIT is CAI.

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Other records listing Draeger Medical, 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.

K042607PRIMUS USK042419FABIUS GS/FABIUS TIRO ANESTHESIA SYSTEMK042276D-VAPORK042086FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEMK041622MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEMK040847MODIFICATION TO VAMOS ANESTHETIC GAS MONITOR

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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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