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FDA 510(k)

FLEXGUIDE

K-Number: K940799 · 1994-08-18

ApplicantScientific Sales Intl., Inc.
Decision Date1994-08-18
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLEXGUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Sales Intl., Inc.. It received FDA 510(k) clearance on 1994-08-18 under 510(k) number K940799. 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 FLEXGUIDE?

FLEXGUIDE is a medical device that received FDA 510(k) clearance on 1994-08-18. The listed applicant is Scientific Sales Intl., Inc.. The 510(k) number is K940799.

When did FLEXGUIDE receive FDA 510(k) clearance?

FLEXGUIDE received FDA 510(k) clearance on 1994-08-18, under 510(k) number K940799.

Who is the listed applicant for FLEXGUIDE?

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

What is the FDA product code for FLEXGUIDE?

The FDA product code for FLEXGUIDE is BSR.

Related Clinical Trials

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Other records listing Scientific Sales 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.

K953677LIGHTED FLEXGUIDE (MODIFICATION)K860996SANASSAY IC TESTK862087SANTEST 1APK861336IAP PLATE TESTK853285MYWASHER 5K853284MYREADER 7

View all 11 devices →

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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