Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RDP-2

K-Number: K961922 · 1996-08-09

ApplicantRanfac, Corp.
Decision Date1996-08-09
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RDP-2 is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac, Corp.. It received FDA 510(k) clearance on 1996-08-09 under 510(k) number K961922. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RDP-2?

RDP-2 is a medical device that received FDA 510(k) clearance on 1996-08-09. The listed applicant is Ranfac, Corp.. The 510(k) number is K961922.

When did RDP-2 receive FDA 510(k) clearance?

RDP-2 received FDA 510(k) clearance on 1996-08-09, under 510(k) number K961922.

Who is the listed applicant for RDP-2?

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 RDP-2?

The FDA product code for RDP-2 is HET.

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 THROWK951090INTRODUCERK930474NEEDLE, PNEUMOPERITONEUM, SPRING LOADED

View all 9 devices →

Related Devices (Code: HET)

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.

K250939SIRIUS Endoscope System (PR-SI-1230)Precision Robotics (Hong Kong) LimitedK243821i-CutA.M.I. Agency For Medical Innovations GmbHK221642SIRIUS Endoscope SystemPrecision Robotics (Hong Kong) LimitedK210116Video Endoscopy System, 3D Video Endoscopy SystemSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.K201832Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5Olympus Medical Systems Corp.K210104SurroundScope System270surgical , Ltd.

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.

↑