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FDA 510(k)

SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY

K-Number: K874665 · 1988-01-20

ApplicantPrecision Dynamics Corp.
Decision Date1988-01-20
Product CodeLRP
Advisory CommitteeSU
DecisionUnknown

Device Summary

SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY 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 1988-01-20 under 510(k) number K874665. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY?

SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY is a medical device that received FDA 510(k) clearance on 1988-01-20. The listed applicant is Precision Dynamics Corp.. The 510(k) number is K874665.

When did SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY receive FDA 510(k) clearance?

SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY received FDA 510(k) clearance on 1988-01-20, under 510(k) number K874665.

Who is the listed applicant for SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY?

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 FINE NEEDLE ASPIRATION BIOPSY TRAY?

The FDA product code for SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY is LRP.

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Other records listing Precision Dynamics Corp. 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.

K020718SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILEK994353SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565K994263SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540K990737'ECURLINE UMBILICAL CORD CLAMP #3500K884357PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEMK882580MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE

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Related Devices (Code: LRP)

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.

K963723LACERATION TRAYGrand Medical ProductsK951811OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACKOsteotech, Inc.K940239EYE TRAYCush Medical ProductsK935621CUSTOM ENT PACKSAssociated MedicalK940646ORTHOPEDIC TRAY PRODUCT LINECushinduK940444GENERAL SURGERY TRAYCush Medical Products

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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