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FDA 510(k)

ACCESS EXPANSION SYSTEM

K-Number: K951894 · 1995-06-15

ApplicantMicro-Medical Devices, Inc.
Decision Date1995-06-15
Product CodeFHO
Advisory CommitteeGU
DecisionUnknown

Device Summary

ACCESS EXPANSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Medical Devices, Inc.. It received FDA 510(k) clearance on 1995-06-15 under 510(k) number K951894. The device is classified under product code FHO. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ACCESS EXPANSION SYSTEM?

ACCESS EXPANSION SYSTEM is a medical device that received FDA 510(k) clearance on 1995-06-15. The listed applicant is Micro-Medical Devices, Inc.. The 510(k) number is K951894.

When did ACCESS EXPANSION SYSTEM receive FDA 510(k) clearance?

ACCESS EXPANSION SYSTEM received FDA 510(k) clearance on 1995-06-15, under 510(k) number K951894.

Who is the listed applicant for ACCESS EXPANSION SYSTEM?

The FDA 510(k) record lists Micro-Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCESS EXPANSION SYSTEM?

The FDA product code for ACCESS EXPANSION SYSTEM is FHO.

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Other records listing Micro-Medical Devices, Inc. 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.

K003695MICROSCOPE-STAINLESS STEEL/FIBER OPTIC: .5-2.6MM MODEL MMD 4500 SERIES AND 2.7-5.0MM MODEL MMD-4700 SERIESK983882MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400K963675THE FLAT PANEL STEIRLE DRAPE SYSTEM(TM), VIDEO MONITOR STERILE DRAPEK951482ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE)K945656THE COUPLER/DRAPE(TM), VIDEO CAMERA STERILE DRAPEK940141LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH

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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.K943624ELMED PNEUMOPERITONEUM NEEDLESHenke-Sass, Wolf GmbH

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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