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FDA 510(k)

SIGNAPAD

K-Number: K780973 · 1978-07-27

ApplicantParker Laboratories, Inc.
Decision Date1978-07-27
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SIGNAPAD is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K780973. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGNAPAD?

SIGNAPAD is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K780973.

When did SIGNAPAD receive FDA 510(k) clearance?

SIGNAPAD received FDA 510(k) clearance on 1978-07-27, under 510(k) number K780973.

Who is the listed applicant for SIGNAPAD?

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

What is the FDA product code for SIGNAPAD?

The FDA product code for SIGNAPAD is GYB.

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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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