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FDA 510(k)

BOUNDARY TUBING HOLDERS

K-Number: K810888 · 1981-04-23

ApplicantThe Buckeye Cellulose Corp.
Decision Date1981-04-23
Product CodeFZX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BOUNDARY TUBING HOLDERS is the device name listed in this FDA 510(k) record. The listed applicant is The Buckeye Cellulose Corp.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810888. The device is classified under product code FZX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOUNDARY TUBING HOLDERS?

BOUNDARY TUBING HOLDERS is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is The Buckeye Cellulose Corp.. The 510(k) number is K810888.

When did BOUNDARY TUBING HOLDERS receive FDA 510(k) clearance?

BOUNDARY TUBING HOLDERS received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810888.

Who is the listed applicant for BOUNDARY TUBING HOLDERS?

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

What is the FDA product code for BOUNDARY TUBING HOLDERS?

The FDA product code for BOUNDARY TUBING HOLDERS is FZX.

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Other records listing The Buckeye Cellulose 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.

K822925BOUNDARY SINGLE-USE GOWNSK823173ARRIRM SCRUB BRUSH/SPONGEK821564BOUNDARY PROCESS CHANGEK820758BOUNDARY SINGLE-USE CRANIOTOMY SHEETK820116BOUNDARYK813450BOUNDARY SINGLE-USE DRAPES

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Related Devices (Code: FZX)

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.

K914715PARALLELING GUIDESImplant Corp. of AmericaK871413CIVCO STEPPERCIVCO Medical Instruments Co., Inc.K871503BIOPSY NEEDLE GUIDE KIT, STERILEAmedic USAK862564A.C.L. GUIDE KITAspen Laboratories, Inc.K854262MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLYMeadox Surgimed, Inc.K852402NAMIC HOMER MAMMALOK NEEDLE/WIRE LOCALIZERNorth American Instrument Corp.

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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