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FDA 510(k)

MINISTIK MINI PUNCTURE SET CATALOG CODE #57505

K-Number: K871137 · 1987-07-16

ApplicantDlp, Inc.
Decision Date1987-07-16
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINISTIK MINI PUNCTURE SET CATALOG CODE #57505 is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K871137. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINISTIK MINI PUNCTURE SET CATALOG CODE #57505?

MINISTIK MINI PUNCTURE SET CATALOG CODE #57505 is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Dlp, Inc.. The 510(k) number is K871137.

When did MINISTIK MINI PUNCTURE SET CATALOG CODE #57505 receive FDA 510(k) clearance?

MINISTIK MINI PUNCTURE SET CATALOG CODE #57505 received FDA 510(k) clearance on 1987-07-16, under 510(k) number K871137.

Who is the listed applicant for MINISTIK MINI PUNCTURE SET CATALOG CODE #57505?

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

What is the FDA product code for MINISTIK MINI PUNCTURE SET CATALOG CODE #57505?

The FDA product code for MINISTIK MINI PUNCTURE SET CATALOG CODE #57505 is DQX.

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Other records listing Dlp, Inc. as applicant

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Related Devices (Code: DQX)

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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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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