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FDA 510(k)

QUICK PRIME LINES, #'S BPL-12, BPL-48 &

K-Number: K802378 · 1980-10-10

ApplicantBentley Laboratories, Inc.
Decision Date1980-10-10
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUICK PRIME LINES, #'S BPL-12, BPL-48 & is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802378. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK PRIME LINES, #'S BPL-12, BPL-48 &?

QUICK PRIME LINES, #'S BPL-12, BPL-48 & is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K802378.

When did QUICK PRIME LINES, #'S BPL-12, BPL-48 & receive FDA 510(k) clearance?

QUICK PRIME LINES, #'S BPL-12, BPL-48 & received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802378.

Who is the listed applicant for QUICK PRIME LINES, #'S BPL-12, BPL-48 &?

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

What is the FDA product code for QUICK PRIME LINES, #'S BPL-12, BPL-48 &?

The FDA product code for QUICK PRIME LINES, #'S BPL-12, BPL-48 & is DWF.

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Other records listing Bentley Laboratories, 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.

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Related Devices (Code: DWF)

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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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