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FDA 510(k)

STERILE LEMAITRE GLOW 'N TELL TAPE

K-Number: K932184 · 1993-07-22

ApplicantVascutech, Inc.
Decision Date1993-07-22
Product CodeKFX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STERILE LEMAITRE GLOW 'N TELL TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Vascutech, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K932184. The device is classified under product code KFX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE LEMAITRE GLOW 'N TELL TAPE?

STERILE LEMAITRE GLOW 'N TELL TAPE is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Vascutech, Inc.. The 510(k) number is K932184.

When did STERILE LEMAITRE GLOW 'N TELL TAPE receive FDA 510(k) clearance?

STERILE LEMAITRE GLOW 'N TELL TAPE received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932184.

Who is the listed applicant for STERILE LEMAITRE GLOW 'N TELL TAPE?

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

What is the FDA product code for STERILE LEMAITRE GLOW 'N TELL TAPE?

The FDA product code for STERILE LEMAITRE GLOW 'N TELL TAPE is KFX.

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Other records listing Vascutech, 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.

K001621DARDIK CAROTID SHUNTK992942LEMAITRE OCCLUSION CATHETERK992933LEMAITRE IRRIGATION CATHETERK992934LEMAITRE VENOUS THROMBECTOMY CATHETERK992940LEMAITRE BALLOON CATHETER WITH IRRIGATIONK992941LEMAITRE BILIARY CATHETER

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Related Devices (Code: KFX)

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.

K833868IPOS G.L.P. SYSTEMIpos LuneburgK830285REGNELL HYDRAULIC FEMORAL PROTHESISBesco Financial ServiceK822240ETHYLENE OXIDE STERILIZ. PARAMETRIC REL.American Mcgaw

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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