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FDA 510(k)

PINSET

K-Number: K884970 · 1989-09-07

ApplicantSafety Diagnostics, Inc.
Decision Date1989-09-07
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PINSET is the device name listed in this FDA 510(k) record. The listed applicant is Safety Diagnostics, Inc.. It received FDA 510(k) clearance on 1989-09-07 under 510(k) number K884970. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PINSET?

PINSET is a medical device that received FDA 510(k) clearance on 1989-09-07. The listed applicant is Safety Diagnostics, Inc.. The 510(k) number is K884970.

When did PINSET receive FDA 510(k) clearance?

PINSET received FDA 510(k) clearance on 1989-09-07, under 510(k) number K884970.

Who is the listed applicant for PINSET?

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

What is the FDA product code for PINSET?

The FDA product code for PINSET is JKA.

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Related Devices (Code: JKA)

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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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