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)

#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES

K-Number: K910781 · 1991-05-15

ApplicantMidmark Corp.
Decision Date1991-05-15
Product CodeETF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1991-05-15 under 510(k) number K910781. The device is classified under product code ETF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the #491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES?

#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES is a medical device that received FDA 510(k) clearance on 1991-05-15. The listed applicant is Midmark Corp.. The 510(k) number is K910781.

When did #491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES receive FDA 510(k) clearance?

#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES received FDA 510(k) clearance on 1991-05-15, under 510(k) number K910781.

Who is the listed applicant for #491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES?

The FDA 510(k) record lists Midmark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for #491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES?

The FDA product code for #491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES is ETF.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Midmark 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.

K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CK112380CLEARVISIONK090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERK023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERK003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMK992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZER

View all 31 devices →

Related Devices (Code: ETF)

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.

K953457JEDMED SPECTRUM ENT CABINETJedmed Instrument Co.K945395PREMIER MIRROR WARMERPremier Dental Products Co.K932470LANGGASSE 90Happersberger Otopront GmbHK911901MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCEStortzK910243MOBILE TREATMENT CARTJedmed Instrument Co.K896298JEDMED S CHAIRJedmed Instrument Co.

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.

↑