FDA 510(k)

SYNERGIST POWER PACK

K-Number: K960414 · 1996-04-24

Decision Date1996-04-24

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

SYNERGIST POWER PACK is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1996-04-24 under 510(k) number K960414. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNERGIST POWER PACK?

SYNERGIST POWER PACK is a medical device that received FDA 510(k) clearance on 1996-04-24. The listed applicant is Chiron Vision Corp.. The 510(k) number is K960414.

When did SYNERGIST POWER PACK receive FDA 510(k) clearance?

SYNERGIST POWER PACK received FDA 510(k) clearance on 1996-04-24, under 510(k) number K960414.

Who is the listed applicant for SYNERGIST POWER PACK?

The FDA 510(k) record lists Chiron Vision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNERGIST POWER PACK?

The FDA product code for SYNERGIST POWER PACK is HQC.

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Related Devices (Code: HQC)

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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.