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FDA 510(k)

SS-1000 POLYGRAPH

K-Number: K872520 · 1988-04-19

ApplicantMeramed Corp.
Decision Date1988-04-19
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SS-1000 POLYGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Meramed Corp.. It received FDA 510(k) clearance on 1988-04-19 under 510(k) number K872520. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SS-1000 POLYGRAPH?

SS-1000 POLYGRAPH is a medical device that received FDA 510(k) clearance on 1988-04-19. The listed applicant is Meramed Corp.. The 510(k) number is K872520.

When did SS-1000 POLYGRAPH receive FDA 510(k) clearance?

SS-1000 POLYGRAPH received FDA 510(k) clearance on 1988-04-19, under 510(k) number K872520.

Who is the listed applicant for SS-1000 POLYGRAPH?

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

What is the FDA product code for SS-1000 POLYGRAPH?

The FDA product code for SS-1000 POLYGRAPH is DQA.

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Related Devices (Code: DQA)

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

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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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