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FDA 510(k)

DRYDEN SCAVENGER INTERFACE SYSTEM

K-Number: K842843 · 1984-07-27

ApplicantDryden Corp.
Decision Date1984-07-27
Product Code
DecisionSubstantially Equivalent

Device Summary

DRYDEN SCAVENGER INTERFACE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1984-07-27 under 510(k) number K842843. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRYDEN SCAVENGER INTERFACE SYSTEM?

DRYDEN SCAVENGER INTERFACE SYSTEM is a medical device that received FDA 510(k) clearance on 1984-07-27. The listed applicant is Dryden Corp.. The 510(k) number is K842843.

When did DRYDEN SCAVENGER INTERFACE SYSTEM receive FDA 510(k) clearance?

DRYDEN SCAVENGER INTERFACE SYSTEM received FDA 510(k) clearance on 1984-07-27, under 510(k) number K842843.

Who is the listed applicant for DRYDEN SCAVENGER INTERFACE SYSTEM?

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

Related Clinical Trials

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Other records listing Dryden Corp. 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.

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

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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.

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