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FDA 510(k)

SYNERGY II

K-Number: K942445 · 1994-11-22

ApplicantSynectics Medical, Inc.
Decision Date1994-11-22
Product CodeMMZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYNERGY II is the device name listed in this FDA 510(k) record. The listed applicant is Synectics Medical, Inc.. It received FDA 510(k) clearance on 1994-11-22 under 510(k) number K942445. The device is classified under product code MMZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNERGY II?

SYNERGY II is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Synectics Medical, Inc.. The 510(k) number is K942445.

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

SYNERGY II received FDA 510(k) clearance on 1994-11-22, under 510(k) number K942445.

Who is the listed applicant for SYNERGY II?

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

What is the FDA product code for SYNERGY II?

The FDA product code for SYNERGY II is MMZ.

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Other records listing Synectics Medical, 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.

K963330URODYNAMIC ANALYSIS MODULEK961070ESOPHAGEAL MANOMETRY ANALYSIS MODULEK951442FLOLABK946322POLYGRAM SOFTWARE

Related Devices (Code: MMZ)

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.

K033335LITHOSTAR MODULARIS WITH SHOCKWAVE SYSTEM CPLUSSiemens Medical Solutions USA, Inc.K954278BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005Beta Medical Products, Inc.K942485MDT UROLOGY TABLEMdt Corp., Inc.

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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