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FDA 510(k)

UNIVERSAL CONTROL ARM

K-Number: K833871 · 1983-12-27

ApplicantAnesthesia Assoc., Inc.
Decision Date1983-12-27
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL CONTROL ARM is the device name listed in this FDA 510(k) record. The listed applicant is Anesthesia Assoc., Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833871. 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 UNIVERSAL CONTROL ARM?

UNIVERSAL CONTROL ARM is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Anesthesia Assoc., Inc.. The 510(k) number is K833871.

When did UNIVERSAL CONTROL ARM receive FDA 510(k) clearance?

UNIVERSAL CONTROL ARM received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833871.

Who is the listed applicant for UNIVERSAL CONTROL ARM?

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

What is the FDA product code for UNIVERSAL CONTROL ARM?

The FDA product code for UNIVERSAL CONTROL ARM is CAI.

Related Clinical Trials

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Other records listing Anesthesia Assoc., 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.

K921926JET VENTILATOR/JETTING DEVICEK811614NERVE STIMULATOR MODEL AA 1050

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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