FDA 510(k)

SECURLINE FRANSEENE NEEDLE

K-Number: K873369 · 1987-10-20

Decision Date1987-10-20

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SECURLINE FRANSEENE NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Precision Dynamics Corp.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K873369. 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 SECURLINE FRANSEENE NEEDLE?

SECURLINE FRANSEENE NEEDLE is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Precision Dynamics Corp.. The 510(k) number is K873369.

When did SECURLINE FRANSEENE NEEDLE receive FDA 510(k) clearance?

SECURLINE FRANSEENE NEEDLE received FDA 510(k) clearance on 1987-10-20, under 510(k) number K873369.

Who is the listed applicant for SECURLINE FRANSEENE NEEDLE?

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

What is the FDA product code for SECURLINE FRANSEENE NEEDLE?

The FDA product code for SECURLINE FRANSEENE NEEDLE is KNW.

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Other records listing Precision Dynamics Corp. as applicant

K020718SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE K994353SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565 K994263SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540 K990737'ECURLINE UMBILICAL CORD CLAMP #3500 K884357PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM K882580MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE

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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.