Atlas FDA

INDXTM DIP-S-TICKSTM

FDA 510(k) clearance K920569 · decided 1993-02-09

Clearance details

K-number
K920569
Device name
INDXTM DIP-S-TICKSTM
Applicant
Intercare Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1992-02-07
Decision date
1993-02-09
Days to decision
368 days
Clearance type
Traditional
Product code
LSQ
Device class
1
Regulation number
866.3500
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Baltimore, MD, 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
INDX DIP-S-TICKS SCRUB TYPHUS TEST FOR THE DETECTION OF IGG AND IGM ANTIBODIES TO ORIENTIA TSUTSUGAMUSHI (SCRUB TYPHUS) (K971591)David C. Bishop, Ph.D.1998-03-13
INDX DIP S TICKS (K901597)Intercare Diagnostics, Inc.1990-12-21
LATEX R. CONORII (K872129)Health Research, Inc.1987-08-19

Recalls involving this device

No recalls on record reference this clearance.