Pacific Biotech, Inc.
Pacific Biotech, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1993.
Top product codes for Pacific Biotech, Inc.
Recent clearances by Pacific Biotech, Inc.
- K924461 — STREP A NEGATIVE CONTROL
- K902510 — CARDS O.S. MONO
- K896482 — PERFECT(TM) ONE STEP EARLY PREGNANCY TEST KIT
- K896221 — CARDS O.S.(TM) STREP A
- K895390 — CARDS O.S. (TM) HCG-URINE
- K891770 — HCG IRMA II
- K884616 — FIRSTDAY EARLY PREGNANCY TESTING KIT II
- K883742 — MODIFIED TSH IRMA KIT
- K884007 — CARDS(TM) MONO
- K882895 — MODIFIED BETA QUIK STAT EIA KIT
- K883639 — MODIFIED HCG IRMA KIT
- K881015 — FIRSTDAY(TM) EARLY PREGNANCY TESTING KIT
- K873788 — CARDS(TM) HCG-SERUM/URINE CR-7503 AND CR-7504
- K863341 — CARDS(TM) - EARLY PREGNANCY TEST
- K863647 — CARDS(TM) STREP A CATALOG NO. CR-7545
- K863199 — CARDS(TM) HCG-URINE
- K862007 — HCG IRMA, CAT. NO. CR-1501
- K862249 — TSH IRMA KIT
- K861575 — DIRECTATEX STREP A
- K860945 — DIRECTACLONE CG SLIDE PREGNANCY TEST
- K860965 — BETA QUIK STICK
- K852327 — BETA QUIK STAT
- K850383 — PRL QUIK RIA KIT
- K843795 — BETA QUIK V
- K843545 — TSH QUIK RIA KIT
- K840230 — FSH QUIK RIA KIT
- K840174 — LH QUIK RIA KIT
- K831302 — PBI BHCG RIA KIT
- K831223 — BETA-QUIK-15 RIA KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.