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FDA 510(k)

MULTIPICS(ME-977)

K-Number: K971154 · 1997-06-25

ApplicantMerlin Engineering Works, Inc.
Decision Date1997-06-25
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIPICS(ME-977) is the device name listed in this FDA 510(k) record. The listed applicant is Merlin Engineering Works, Inc.. It received FDA 510(k) clearance on 1997-06-25 under 510(k) number K971154. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPICS(ME-977)?

MULTIPICS(ME-977) is a medical device that received FDA 510(k) clearance on 1997-06-25. The listed applicant is Merlin Engineering Works, Inc.. The 510(k) number is K971154.

When did MULTIPICS(ME-977) receive FDA 510(k) clearance?

MULTIPICS(ME-977) received FDA 510(k) clearance on 1997-06-25, under 510(k) number K971154.

Who is the listed applicant for MULTIPICS(ME-977)?

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

What is the FDA product code for MULTIPICS(ME-977)?

The FDA product code for MULTIPICS(ME-977) is LMD.

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Other records listing Merlin Engineering Works, Inc. as applicant

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.

K974882DOWNSCAN LTK971153SPLITSCREEN (ME-975)K970451DOWNSCAN 120K970450UPSCAN 120K954211CRISPICSK953398UNISCAN

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Related Devices (Code: LMD)

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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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