# Acro Biotech, LLC

- Location (FDA's records): Rancho Cucamonga, CA
- FDA decisions: 10 (2006–2018): 10 510(k) clearances
- Names in FDA's records: Acro Biotech, LLC (8); Acro Biotech, Inc. (2)
- Product codes: DJC (2), LCX (2), DIO (1), DKZ (1), JXM (1), LCM (1), LDJ (1), DJG (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Vanguard Biomedical Corp.: 1 (https://510kreport.com/company/vanguard-biomedical)

## Its most-cited devices
- K172512: ACRO HCG Pregnancy Rapid Test (2018), cited by 1

## Recent decisions
- K180771: Acro HCG Pregnancy Rapid Test (May 18, 2018)
- K172512: ACRO HCG Pregnancy Rapid Test (Feb 2, 2018)
- K060355: Acro Biotech LLC Rapid Mdma Urine Test, Catalog MDMA0010000 (Aug 7, 2006)
- K060354: Acro Biotech LLC Rapid Benzodiazepine Urine Test, Catalog BZD001000 (Jul 28, 2006)
- K053037: Acro Biotech LLC Rapid Opiates Urine Test; Catalog# OPI00100 (Jun 15, 2006)
- K053033: Acro Biotech LLC Rapid Methamphetamine Urine Test; Catalog# MET001000 (Jun 6, 2006)
- K053034: Acro Biotech LLC Rapid Tetrahydrocannabinol Urine Test; Catalog# OPI001000 (Jun 6, 2006)
- K053035: Acro Biotech LLC Rapid Benzoylecgonine Urine Test; Catalog# MET001000 (May 5, 2006)

Source page: https://510kreport.com/company/acro-biotech