FDA 510(k)

MANAN TURNER STYLE NEEDLE

K-Number: K873208 · 1987-08-25

Decision Date1987-08-25

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MANAN TURNER STYLE 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 1987-08-25 under 510(k) number K873208. 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 TURNER STYLE NEEDLE?

MANAN TURNER STYLE NEEDLE is a medical device that received FDA 510(k) clearance on 1987-08-25. The listed applicant is Manan Manufacturing Co., Inc.. The 510(k) number is K873208.

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

MANAN TURNER STYLE NEEDLE received FDA 510(k) clearance on 1987-08-25, under 510(k) number K873208.

Who is the listed applicant for MANAN TURNER STYLE 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 TURNER STYLE NEEDLE?

The FDA product code for MANAN TURNER STYLE NEEDLE is KNW.

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Other records listing Manan Manufacturing Co., Inc. as applicant

K864405MANAN CONTRAST MEDIA ADMINISTRATION SET K863848MANAN BREST TUMOR LOCALIZATION NEEDLE K852018ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHR K851832NAMAN POTTS COURNAND NEEDLE K852501MYELOGRAM PROCEDURE TRAY K851834MANAN GWI GUIDE WIRE INTRODUCER

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Related Devices (Code: KNW)

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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.