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FDA 510(k)

MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES

K-Number: K030857 · 2003-10-16

ApplicantMahe Intl., Inc.
Decision Date2003-10-16
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Mahe Intl., Inc.. It received FDA 510(k) clearance on 2003-10-16 under 510(k) number K030857. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES?

MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES is a medical device that received FDA 510(k) clearance on 2003-10-16. The listed applicant is Mahe Intl., Inc.. The 510(k) number is K030857.

When did MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES receive FDA 510(k) clearance?

MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES received FDA 510(k) clearance on 2003-10-16, under 510(k) number K030857.

Who is the listed applicant for MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES?

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

What is the FDA product code for MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES?

The FDA product code for MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES is EOB.

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Other records listing Mahe Intl., 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.

K991426MAHE INSTRUMENTSK942823MAHE INSTRUMENTS

Related Devices (Code: EOB)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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