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FDA 510(k)

WILLIAMS ACS MARKER NEEDLE

K-Number: K882036 · 1988-07-27

ApplicantBuckman Co., Inc.
Decision Date1988-07-27
Product CodeGDF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WILLIAMS ACS MARKER NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1988-07-27 under 510(k) number K882036. The device is classified under product code GDF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAMS ACS MARKER NEEDLE?

WILLIAMS ACS MARKER NEEDLE is a medical device that received FDA 510(k) clearance on 1988-07-27. The listed applicant is Buckman Co., Inc.. The 510(k) number is K882036.

When did WILLIAMS ACS MARKER NEEDLE receive FDA 510(k) clearance?

WILLIAMS ACS MARKER NEEDLE received FDA 510(k) clearance on 1988-07-27, under 510(k) number K882036.

Who is the listed applicant for WILLIAMS ACS MARKER NEEDLE?

The FDA 510(k) record lists Buckman Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WILLIAMS ACS MARKER NEEDLE?

The FDA product code for WILLIAMS ACS MARKER NEEDLE is GDF.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: GDF)

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.

K031173NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013Needle Tech Products, Inc.K950311GLOBAL MEDICAL PRODUCTS BREST LESION LOCALIZATION NEEDLE WITH STIFFENED WIREGlobal Medical Products, Ltd.K950007SURGICAL INSTRUMENT GUIDEUnited States Surgical, A Division of Tyco HealthcK945124BREAST LESION LOCALIZATION NEEDLEPromex, Inc.K944942BREAST LESION LOCALIZATION NEEDLEPromedical , Ltd.K935538BAUER TEMNO COAXIAL NEEDLEBauer Medical, 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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