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FDA 510(k)

PASCAL MEDICAL AB MENIETT 20

K-Number: K991562 · 1999-12-28

ApplicantPascal Medical AB
Decision Date1999-12-28
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PASCAL MEDICAL AB MENIETT 20 is the device name listed in this FDA 510(k) record. The listed applicant is Pascal Medical AB. It received FDA 510(k) clearance on 1999-12-28 under 510(k) number K991562. The device is classified under product code ETY. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PASCAL MEDICAL AB MENIETT 20?

PASCAL MEDICAL AB MENIETT 20 is a medical device that received FDA 510(k) clearance on 1999-12-28. The listed applicant is Pascal Medical AB. The 510(k) number is K991562.

When did PASCAL MEDICAL AB MENIETT 20 receive FDA 510(k) clearance?

PASCAL MEDICAL AB MENIETT 20 received FDA 510(k) clearance on 1999-12-28, under 510(k) number K991562.

Who is the listed applicant for PASCAL MEDICAL AB MENIETT 20?

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

What is the FDA product code for PASCAL MEDICAL AB MENIETT 20?

The FDA product code for PASCAL MEDICAL AB MENIETT 20 is ETY.

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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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