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FDA 510(k)

CORRUGATED TUBING, 770 & 771

K-Number: K770581 · 1977-04-19

ApplicantC.D. & F. Corp.
Decision Date1977-04-19
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CORRUGATED TUBING, 770 & 771 is the device name listed in this FDA 510(k) record. The listed applicant is C.D. & F. Corp.. It received FDA 510(k) clearance on 1977-04-19 under 510(k) number K770581. 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 CORRUGATED TUBING, 770 & 771?

CORRUGATED TUBING, 770 & 771 is a medical device that received FDA 510(k) clearance on 1977-04-19. The listed applicant is C.D. & F. Corp.. The 510(k) number is K770581.

When did CORRUGATED TUBING, 770 & 771 receive FDA 510(k) clearance?

CORRUGATED TUBING, 770 & 771 received FDA 510(k) clearance on 1977-04-19, under 510(k) number K770581.

Who is the listed applicant for CORRUGATED TUBING, 770 & 771?

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

What is the FDA product code for CORRUGATED TUBING, 770 & 771?

The FDA product code for CORRUGATED TUBING, 770 & 771 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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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.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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