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FDA 510(k)

NEEDLE, PNEUMOPERITONEUM, SPRING LOADED

K-Number: K930474 · 1993-07-23

ApplicantRanfac, Corp.
Decision Date1993-07-23
Product CodeFHO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEEDLE, PNEUMOPERITONEUM, SPRING LOADED is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac, Corp.. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K930474. The device is classified under product code FHO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE, PNEUMOPERITONEUM, SPRING LOADED?

NEEDLE, PNEUMOPERITONEUM, SPRING LOADED is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Ranfac, Corp.. The 510(k) number is K930474.

When did NEEDLE, PNEUMOPERITONEUM, SPRING LOADED receive FDA 510(k) clearance?

NEEDLE, PNEUMOPERITONEUM, SPRING LOADED received FDA 510(k) clearance on 1993-07-23, under 510(k) number K930474.

Who is the listed applicant for NEEDLE, PNEUMOPERITONEUM, SPRING LOADED?

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 NEEDLE, PNEUMOPERITONEUM, SPRING LOADED?

The FDA product code for NEEDLE, PNEUMOPERITONEUM, SPRING LOADED is FHO.

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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: FHO)

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.

K172120Veress NeedleWickimed (Huizhou) Medical Equipment Manufacturing Co.,LtdK121370VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLEVectecK010779MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTGibbons Surgical Corp.K970788PNEUMO-MATIC INSUFFLATION NEEDLEApple Medical Corp.K960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMSherwood Medical Co.K951894ACCESS EXPANSION SYSTEMMicro-Medical Devices, 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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