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FDA 510(k)

RANFAC CUT BIOPSY NEEDLE

K-Number: K864139 · 1986-11-05

ApplicantRanfac, Corp.
Decision Date1986-11-05
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RANFAC CUT BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac, Corp.. It received FDA 510(k) clearance on 1986-11-05 under 510(k) number K864139. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RANFAC CUT BIOPSY NEEDLE?

RANFAC CUT BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1986-11-05. The listed applicant is Ranfac, Corp.. The 510(k) number is K864139.

When did RANFAC CUT BIOPSY NEEDLE receive FDA 510(k) clearance?

RANFAC CUT BIOPSY NEEDLE received FDA 510(k) clearance on 1986-11-05, under 510(k) number K864139.

Who is the listed applicant for RANFAC CUT BIOPSY NEEDLE?

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

What is the FDA product code for RANFAC CUT BIOPSY NEEDLE?

The FDA product code for RANFAC CUT BIOPSY NEEDLE is GAA.

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Other records listing Ranfac, 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.

K162932Ranfac Fat Aspiration CannulaK131157RANFAC BONE MARROW ASPIRATION NEEDLEK031344RANFAC GOLDENBERG SNARECOIL SOFT TISSUE BIOPSY (GSS) NEEDLEK012224SINGLE ACTION BIOPSY NEEDLE, MODEL RCBS: XX GAUGE, XX LENGTH, XX THROWK961922RDP-2K951090INTRODUCER

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Related Devices (Code: GAA)

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.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN ACCURA NEEDLEMedical Device Technologies, Inc.

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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