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FDA 510(k)

MANAN WESTCOTT NEEDLE

K-Number: K851837 · 1985-05-14

ApplicantManan Manufacturing Co., Inc.
Decision Date1985-05-14
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MANAN WESTCOTT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Manan Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1985-05-14 under 510(k) number K851837. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANAN WESTCOTT NEEDLE?

MANAN WESTCOTT NEEDLE is a medical device that received FDA 510(k) clearance on 1985-05-14. The listed applicant is Manan Manufacturing Co., Inc.. The 510(k) number is K851837.

When did MANAN WESTCOTT NEEDLE receive FDA 510(k) clearance?

MANAN WESTCOTT NEEDLE received FDA 510(k) clearance on 1985-05-14, under 510(k) number K851837.

Who is the listed applicant for MANAN WESTCOTT NEEDLE?

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

What is the FDA product code for MANAN WESTCOTT NEEDLE?

The FDA product code for MANAN WESTCOTT NEEDLE is KNW.

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Other records listing Manan Manufacturing Co., Inc. 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.

K873208MANAN TURNER STYLE NEEDLEK864405MANAN CONTRAST MEDIA ADMINISTRATION SETK863848MANAN BREST TUMOR LOCALIZATION NEEDLEK852018ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHRK852501MYELOGRAM PROCEDURE TRAYK851832NAMAN POTTS COURNAND NEEDLE

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Related Devices (Code: KNW)

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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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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