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FDA 510(k)

GRASPERS

K-Number: K935382 · 1994-02-15

ApplicantMectra Labs, Inc.
Decision Date1994-02-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GRASPERS is the device name listed in this FDA 510(k) record. The listed applicant is Mectra Labs, Inc.. It received FDA 510(k) clearance on 1994-02-15 under 510(k) number K935382. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASPERS?

GRASPERS is a medical device that received FDA 510(k) clearance on 1994-02-15. The listed applicant is Mectra Labs, Inc.. The 510(k) number is K935382.

When did GRASPERS receive FDA 510(k) clearance?

GRASPERS received FDA 510(k) clearance on 1994-02-15, under 510(k) number K935382.

Who is the listed applicant for GRASPERS?

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

What is the FDA product code for GRASPERS?

The FDA product code for GRASPERS is GCJ.

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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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