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FDA 510(k)

PTFE SYRINGE FILTER

K-Number: K952918 · 1995-09-15

ApplicantB.Braun Medical, Inc.
Decision Date1995-09-15
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PTFE SYRINGE FILTER is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 1995-09-15 under 510(k) number K952918. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PTFE SYRINGE FILTER?

PTFE SYRINGE FILTER is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K952918.

When did PTFE SYRINGE FILTER receive FDA 510(k) clearance?

PTFE SYRINGE FILTER received FDA 510(k) clearance on 1995-09-15, under 510(k) number K952918.

Who is the listed applicant for PTFE SYRINGE FILTER?

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

What is the FDA product code for PTFE SYRINGE FILTER?

The FDA product code for PTFE SYRINGE FILTER is FMF.

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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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