Atlas FDA

EASTERCLAVE

FDA 510(k) clearance K961230 · decided 1996-06-27

Clearance details

K-number
K961230
Device name
EASTERCLAVE
Applicant
Easter Services, Inc.
Decision
Substantially Equivalent
Date received
1996-03-29
Decision date
1996-06-27
Days to decision
90 days
Clearance type
Traditional
Product code
FLE
Device class
2
Regulation number
880.6880
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Milan, 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
AMSCO 700 Steam Sterilizer (K261055)STERIS Corporation2026-06-24
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Life Ultra 25L Tabletop Mono Chamber Steam Sterilizer (K250168)Lucas Lifecare2025-12-30
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FRONT-LINE Field Sterilizer (FL135) (K243801)Fort Defiance Industries, LLC2025-03-07
Midmark Smart M9® Sterilizer, Midmark Smart M11® Sterilizer (K233026)Midmark Corporation2024-04-04
Lexa MINI (RIS-303, RIS-305) (K233504)W&H Sterilization S.R.L.2024-02-08
PRIMUS Healthcare Sterilizer (Model PSS11-HA & PSS11-HB) (K233132)Primus Sterilizer Company, LLC2023-12-19
T-Top 10 & T-Top T-Top 11 (K232658)Tuttnauer U.S.A Co, Ltd.2023-11-27
AMSCO 600 Steam Sterilizer (K232485)Steris2023-09-13

Recalls involving this device

No recalls on record reference this clearance.