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FDA 510(k)

GOODALL LASER TARGETING DEVICE

K-Number: K934626 · 1993-11-19

ApplicantProtectair, Inc.
Decision Date1993-11-19
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GOODALL LASER TARGETING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Protectair, Inc.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K934626. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOODALL LASER TARGETING DEVICE?

GOODALL LASER TARGETING DEVICE is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Protectair, Inc.. The 510(k) number is K934626.

When did GOODALL LASER TARGETING DEVICE receive FDA 510(k) clearance?

GOODALL LASER TARGETING DEVICE received FDA 510(k) clearance on 1993-11-19, under 510(k) number K934626.

Who is the listed applicant for GOODALL LASER TARGETING DEVICE?

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

What is the FDA product code for GOODALL LASER TARGETING DEVICE?

The FDA product code for GOODALL LASER TARGETING DEVICE is JAA.

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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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