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F.f.p.f. Emc

FDA UDI

Class II (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
F.F.P.F. EMC FDA UDI
Generic Name
Electrosurgical system FDA UDI
Device Name
SURGITRON FFPF EMC 110V. WITH AUDIO FDA UDI
Model / Reference
EMC110A FDA UDI
Description
SURGITRON FFPF EMC 110V. WITH AUDIO FDA UDI

Identifiers

Catalog Number
EMC110A FDA UDI
Primary DI / UDI-DI
00841494104900 FDA UDI
510(k) Number
K972072 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical system

F.f.p.f. Emc by Cynosure, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system.

Cleared under the same submission

K972072 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cynosure, LLC

Sources (1)

  • FDA UDI 5fbaf780-5fb1-4529-b5d1-99621f2a3186 35 fields · synced May 30, 2026