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FDA 510(k)

LIGHTED INTUBATION SYLET

K-Number: K932081 · 1993-07-27

ApplicantAaron Medical, Inc.
Decision Date1993-07-27
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIGHTED INTUBATION SYLET is the device name listed in this FDA 510(k) record. The listed applicant is Aaron Medical, Inc.. It received FDA 510(k) clearance on 1993-07-27 under 510(k) number K932081. The device is classified under product code BSR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHTED INTUBATION SYLET?

LIGHTED INTUBATION SYLET is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Aaron Medical, Inc.. The 510(k) number is K932081.

When did LIGHTED INTUBATION SYLET receive FDA 510(k) clearance?

LIGHTED INTUBATION SYLET received FDA 510(k) clearance on 1993-07-27, under 510(k) number K932081.

Who is the listed applicant for LIGHTED INTUBATION SYLET?

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

What is the FDA product code for LIGHTED INTUBATION SYLET?

The FDA product code for LIGHTED INTUBATION SYLET is BSR.

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.

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Other records listing Aaron Medical, 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.

K011929HANDPIECE SHEATH-MODEL #A910K913623SURGICAL ELECTRICAL PENCIL

Related Devices (Code: BSR)

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.

K162729Aintree Intubation Catheter, Arndt Airway Exchange Catheter Set, Cook Airway Exchange Catheter, and Cook Airway Exchange Catheter - Extra Firm With Soft TipCook IncorporatedK962361TRACHLIGHT STYLET AND TRACHEAL LIGHTWANDLaerdal Medical Corp.K954771TRACHLIGHT STYLET & TRACHEAL LIGHTWAND (ORIGINAL APPLICATION NAME: STYLETT & TRACHEAL LIGHTWAND)Laerdal Medical Corp.K943104MOLLOY INTUBATING STYLETTEMolloy Corp.K955238RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLERusch Intl.K953677LIGHTED FLEXGUIDE (MODIFICATION)Scientific Sales Intl., 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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