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FDA 510(k)

REUSEABLE BREATHING TUBES

K-Number: K873927 · 1987-10-20

ApplicantDryden Corp.
Decision Date1987-10-20
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REUSEABLE BREATHING TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K873927. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSEABLE BREATHING TUBES?

REUSEABLE BREATHING TUBES is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Dryden Corp.. The 510(k) number is K873927.

When did REUSEABLE BREATHING TUBES receive FDA 510(k) clearance?

REUSEABLE BREATHING TUBES received FDA 510(k) clearance on 1987-10-20, under 510(k) number K873927.

Who is the listed applicant for REUSEABLE BREATHING TUBES?

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 BREATHING TUBES?

The FDA product code for REUSEABLE BREATHING TUBES is BZO.

Related Clinical Trials

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.

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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 TOURNIQUETK870859BAG-TAIL BLEED VALVEK871386BREATHING CIRCUIT

View all 21 devices →

Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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