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FDA 510(k)

DEKNA-LOK MODEL BP1000V2L

K-Number: K060801 · 2006-05-17

ApplicantTeleflex Medical
Decision Date2006-05-17
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEKNA-LOK MODEL BP1000V2L is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2006-05-17 under 510(k) number K060801. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEKNA-LOK MODEL BP1000V2L?

DEKNA-LOK MODEL BP1000V2L is a medical device that received FDA 510(k) clearance on 2006-05-17. The listed applicant is Teleflex Medical. The 510(k) number is K060801.

When did DEKNA-LOK MODEL BP1000V2L receive FDA 510(k) clearance?

DEKNA-LOK MODEL BP1000V2L received FDA 510(k) clearance on 2006-05-17, under 510(k) number K060801.

Who is the listed applicant for DEKNA-LOK MODEL BP1000V2L?

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

What is the FDA product code for DEKNA-LOK MODEL BP1000V2L?

The FDA product code for DEKNA-LOK MODEL BP1000V2L is GAM.

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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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