Atlas FDA

MICRO CAUTERY

FDA 510(k) clearance K810909 · decided 1981-04-17

Clearance details

K-number
K810909
Device name
MICRO CAUTERY
Applicant
Key Medical, Inc.
Decision
Substantially Equivalent
Date received
1981-04-03
Decision date
1981-04-17
Days to decision
14 days
Clearance type
Traditional
Product code
HAM
Device class
2
Regulation number
878.4400
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Quiver Laparoscopic Extendable (K153472)Itl Corporation Pty, Ltd.2016-06-23
NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M (K000079)Nikomed U.S.A., Inc.2000-02-04
NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY) (K993306)Paladin Medical, Inc.1999-11-03
BERGEN 710 ESU (K945861)Bergen Mfg.1995-03-01
LAPAROSTAT(TM) (K913300)Cook Ob/Gyn1992-04-02
GSU HANDPIECE ADAPTER (K920100)Beacon Laboratories, Inc.1992-02-03
EMC MODEL NO. STATOME 900 (K911353)Emc Industries1991-06-24
ABC HANDPIECE ADAPTER (K901248)Beacon Laboratories, Inc.1990-04-03
LIGHT COAGULATOR LC 250 (K881334)Nk-Optik GmbH1989-11-16
ELECTROSURGICAL COAGULATION SUCTION TUBE (K895337)New England Surgical Instrument Corp.1989-09-15
BEAMER ONE (K894663)Beacon Laboratories, Inc.1989-09-15
B100 DISPOSABLE HANDPIECE (K894762)Beacon Laboratories, Inc.1989-09-15

Recalls involving this device

No recalls on record reference this clearance.