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FDA 510(k)

LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT

K-Number: K932139 · 1993-07-30

ApplicantAaron Medical Industries
Decision Date1993-07-30
Product CodeFSQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT is the device name listed in this FDA 510(k) record. The listed applicant is Aaron Medical Industries. It received FDA 510(k) clearance on 1993-07-30 under 510(k) number K932139. The device is classified under product code FSQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT?

LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Aaron Medical Industries. The 510(k) number is K932139.

When did LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT receive FDA 510(k) clearance?

LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT received FDA 510(k) clearance on 1993-07-30, under 510(k) number K932139.

Who is the listed applicant for LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT?

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

What is the FDA product code for LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT?

The FDA product code for LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFT is FSQ.

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Other records listing Aaron Medical Industries 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.

K062337MODULAR LAPAROSCOPY ACCESSORIES, HANDLE; SISSORS (STRAIGHT AND CURVED); GRASPER (AGGRESSIVE, ALLIS, ATAUMATIC; DISSECTORK061307BOVIE INAFLASH SUTURE REMOVER HANDLE,CHARGER,HANDLE AND CHARGER,KIT,BATTERY PACKK060117BOVIE BUTTON REMOTE HAND SWITCHK022856BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATORK021817AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240VK020579AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03

View all 46 devices →

Related Devices (Code: FSQ)

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.

K930686MIDMARK SURGICAL LIGHTING SYSTEMSMidmark Corp.K922409ALM ILLUMINATOR SERIES LIGHT SYSTEMAlm Surgical Equipment, Inc.K921848BFW WEHMERLITE IV-A FIBER OPTIC SURG. HEADLIGHTAlm Surgical Equipment, Inc.K803067SURG-FLEX 10 LIGHTMedical Products Development, Inc.K810019SURG-FLEX 15 SURGICAL LIGHTMedical Products Development, Inc.K810018SURG-FLEX 5 SURGICAL LIGHTMedical Products Development, 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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