Atlas FDA

PEM-T

FDA 510(k) clearance K830497 · decided 1983-04-05

Clearance details

K-number
K830497
Device name
PEM-T
Applicant
Hedeco
Decision
Substantially Equivalent
Date received
1983-02-16
Decision date
1983-04-05
Days to decision
48 days
Clearance type
Traditional
Product code
JWZ
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Walker, MI, 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
GENZYME OSOM TRICHOMONAS RAPID TEST (K033864)Genzyme Corp.2004-04-02
XENOSTRIP-TV TRICHOMONAS CASSETTE TEST, MODEL C1383.01 (K020595)Xenotope Diagnostics, Inc.2003-02-20
XENOSTRIP-TV TRICHOMONAS DIAGNOSTIC TEST KIT; CATALOG NUMBERS S1383.01, S1383.02 & S1383.03 (K020226)Hellen Professional Services2002-08-22
MERIVIEW TM TRICHOMONAS (K894246)Meridian Diagnostics, Inc.1989-08-15
SUPER DUO (K892802)Mercia Diagnostics , Ltd.1989-06-13
MERIFLUOR(TM) -TRICHOMONAS (K892263)Meridian Diagnostics, Inc.1989-05-24
TRICHOMATE(R) SUPER (K875138)Mercia Diagnostics , Ltd.1988-05-13
TRICHOMONAS DIRECT ENZYME IMMUNOASSAY (K874259)California Integrated Diagnostics, Inc.1987-12-07
MODIFIED TRICHOMONAS DIRECT SPECIMEN TEST KIT (K871279)California Integrated Diagnostics, Inc.1987-04-08
SYNCOR TRICH DIRECT IMMUNOFLUORESCENCE ASSAY (K852665)Syncor Intl. Corp.1985-08-13

Recalls involving this device

No recalls on record reference this clearance.