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FDA 510(k)

ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA

K-Number: K936155 · 1994-04-11

ApplicantMicromedical Devices, Inc.
Decision Date1994-04-11
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Micromedical Devices, Inc.. It received FDA 510(k) clearance on 1994-04-11 under 510(k) number K936155. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA?

ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is Micromedical Devices, Inc.. The 510(k) number is K936155.

When did ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA receive FDA 510(k) clearance?

ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA received FDA 510(k) clearance on 1994-04-11, under 510(k) number K936155.

Who is the listed applicant for ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA?

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

What is the FDA product code for ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA?

The FDA product code for ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA is HIF.

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Other records listing Micromedical 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.

K043287PALMSCAN AP2000; PALMSCAN A2000; PALMSCAN P2000K936195LAPAROSCOPESK936097VIDEO CAMERAS, ENCOSCOPIC AND SURGICALK936086STERILE VIDEO CAMERA COVER AND DRAPEK850791MDI 2000 - PULSE GENERATORK834262TRANS-PACE

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Related Devices (Code: HIF)

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.

K260209ENDOFLATOR+; Smart Smoke EvacuationKarl Storz SE & CO. KGK252584Insufflator (wAlcor C50A, wAlcor C50B, wAlcor C50C, wAlcor C35A, wAlcor C35B, wAlcor C35C)Weyo Surgical Technology , Ltd.K252318Insufflator (OPTO-IFL1000)Guangdong Optomedic Technologies, Inc.K250388ENDOFLATOR +Karl Storz SE & CO. KGK242772AirSurgN Insufflator (10030/AirSurgN)SmartsurgN, Inc.K243527High Flow Insufflation Unit (UHI-4)Olympus Medical Systems Corporation

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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