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FDA 510(k)

REUSEABLE NON-CONDUCTIVE FIXED Y

K-Number: K841455 · 1984-06-11

ApplicantDryden Corp.
Decision Date1984-06-11
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REUSEABLE NON-CONDUCTIVE FIXED Y is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1984-06-11 under 510(k) number K841455. 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 REUSEABLE NON-CONDUCTIVE FIXED Y?

REUSEABLE NON-CONDUCTIVE FIXED Y is a medical device that received FDA 510(k) clearance on 1984-06-11. The listed applicant is Dryden Corp.. The 510(k) number is K841455.

When did REUSEABLE NON-CONDUCTIVE FIXED Y receive FDA 510(k) clearance?

REUSEABLE NON-CONDUCTIVE FIXED Y received FDA 510(k) clearance on 1984-06-11, under 510(k) number K841455.

Who is the listed applicant for REUSEABLE NON-CONDUCTIVE FIXED Y?

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

What is the FDA product code for REUSEABLE NON-CONDUCTIVE FIXED Y?

The FDA product code for REUSEABLE NON-CONDUCTIVE FIXED Y is CAI.

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Other records listing Dryden Corp. as applicant

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K880923PATIENT VENTILATOR ISOLATORK880769BREATHING CIRCUIT W/HEATED WIREK882285NONREBREATHING CIRCUITK873928UNIVERSAL TOURNIQUETK873927REUSEABLE BREATHING TUBESK870859BAG-TAIL BLEED VALVE

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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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