FDA 510(k)

NONREBREATHING CIRCUIT

K-Number: K882285 · 1988-08-16

Decision Date1988-08-16

Product CodeBTM

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

NONREBREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1988-08-16 under 510(k) number K882285. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NONREBREATHING CIRCUIT?

NONREBREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1988-08-16. The listed applicant is Dryden Corp.. The 510(k) number is K882285.

When did NONREBREATHING CIRCUIT receive FDA 510(k) clearance?

NONREBREATHING CIRCUIT received FDA 510(k) clearance on 1988-08-16, under 510(k) number K882285.

Who is the listed applicant for NONREBREATHING CIRCUIT?

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 NONREBREATHING CIRCUIT?

The FDA product code for NONREBREATHING CIRCUIT is BTM.

Related Clinical Trials

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Other records listing Dryden Corp. as applicant

K880923PATIENT VENTILATOR ISOLATOR K880769BREATHING CIRCUIT W/HEATED WIRE K873928UNIVERSAL TOURNIQUET K873927REUSEABLE BREATHING TUBES K870859BAG-TAIL BLEED VALVE K871386BREATHING CIRCUIT

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Related Devices (Code: BTM)

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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.