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FDA 510(k)

SYNERGY LT

K-Number: K981405 · 1998-07-16

ApplicantOxford Instruments, Plc.
Decision Date1998-07-16
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SYNERGY LT is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Instruments, Plc.. It received FDA 510(k) clearance on 1998-07-16 under 510(k) number K981405. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNERGY LT?

SYNERGY LT is a medical device that received FDA 510(k) clearance on 1998-07-16. The listed applicant is Oxford Instruments, Plc.. The 510(k) number is K981405.

When did SYNERGY LT receive FDA 510(k) clearance?

SYNERGY LT received FDA 510(k) clearance on 1998-07-16, under 510(k) number K981405.

Who is the listed applicant for SYNERGY LT?

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

What is the FDA product code for SYNERGY LT?

The FDA product code for SYNERGY LT is GWF.

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Other records listing Oxford Instruments, Plc. as applicant

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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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