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FDA 510(k)

MANAN MADAYAG PTC NEEDLE

K-Number: K851839 · 1985-06-21

ApplicantManan Manufacturing Co., Inc.
Decision Date1985-06-21
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MANAN MADAYAG PTC 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 1985-06-21 under 510(k) number K851839. 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 MADAYAG PTC NEEDLE?

MANAN MADAYAG PTC NEEDLE is a medical device that received FDA 510(k) clearance on 1985-06-21. The listed applicant is Manan Manufacturing Co., Inc.. The 510(k) number is K851839.

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

MANAN MADAYAG PTC NEEDLE received FDA 510(k) clearance on 1985-06-21, under 510(k) number K851839.

Who is the listed applicant for MANAN MADAYAG PTC 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 MADAYAG PTC NEEDLE?

The FDA product code for MANAN MADAYAG PTC NEEDLE is KNW.

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

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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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