Atlas FDA

ACRODISC FILTER ASSEMBLY

FDA 510(k) clearance K802765 · decided 1981-01-21

Clearance details

K-number
K802765
Device name
ACRODISC FILTER ASSEMBLY
Applicant
Gelman Sciences, Inc.
Decision
Substantially Equivalent
Date received
1980-11-04
Decision date
1981-01-21
Days to decision
78 days
Clearance type
Traditional
Product code
FPB
Device class
2
Regulation number
880.5440
Medical specialty
General Hospital
Advisory committee
General Hospital
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
Filter Needle for Single Use (K233277)Hangzhou Qiantang Longyue Biotechnology Co., Ltd.2024-05-10
Cathivex ¿GV filter units (K143583)Merck Millipore , Ltd.2015-08-11
NON-DEHP MICRO-VOLUME EXTENSION SET WITH 0.22 MICRON FILTER (K113227)Baxter Healthcare Corp2011-12-08
ARTERIA BLOOD FILTER (K021293)Arteria Medical Science, Inc.2002-08-22
PALL SUPOR AEF FILTER (K993379)Pall Corp.1999-12-16
0.2 U BACTERIAL FILTER (K974661)Sims Deltec, Inc.1998-02-11
AUTOPRIME (K964283)Arbor Technologies, Inc.1997-01-22
PALL LEA FILTER (LIPID EMULSION FILTER) (I.V. FILTER) (K954331)Pall Biomedical Products Co.1997-01-09
I.V. FILTER SET (K933523)Mediziv Medical Products 1987 , Ltd.1995-05-19
40 MICRON BLOOD TRANSFUSION FILTER (K941628)Douglas Medical Products Corp.1995-02-16
1.2 MICRON AIR ELIMINATING FILTER (K942625)The Medi-Dose Group1994-10-07
PHARMASSURE LARGE VOLUME TRANSFER FILTERS (K943127)Gelman Sciences, Inc.1994-09-29

Recalls involving this device

No recalls on record reference this clearance.