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FDA 510(k)

WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180

K-Number: K932661 · 1996-04-17

ApplicantWhatman Specialty Products, Inc.
Decision Date1996-04-17
Product CodePJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180 is the device name listed in this FDA 510(k) record. The listed applicant is Whatman Specialty Products, Inc.. It received FDA 510(k) clearance on 1996-04-17 under 510(k) number K932661. The device is classified under product code PJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180?

WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180 is a medical device that received FDA 510(k) clearance on 1996-04-17. The listed applicant is Whatman Specialty Products, Inc.. The 510(k) number is K932661.

When did WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180 receive FDA 510(k) clearance?

WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180 received FDA 510(k) clearance on 1996-04-17, under 510(k) number K932661.

Who is the listed applicant for WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180?

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

What is the FDA product code for WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180?

The FDA product code for WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180 is PJC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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