Cleared Traditional

K992915 - ONE-STEP DOUBLE-CHEK PREGNANCY TEST

K992915 is an FDA 510(k) clearance for ONE-STEP DOUBLE-CHEK PREGNANCY TEST, manufactured by Biomedical Products Corp.. The device is a Class 2 Chemistry device with product code JHI cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K992915 · Biomedical Products Corp. · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1999
Decision
80d
Days
Class 2
Risk

K992915 is an FDA 510(k) clearance for the ONE-STEP DOUBLE-CHEK PREGNANCY TEST. Classified as Visual, Pregnancy Hcg, Prescription Use (product code JHI), Class II - Special Controls.

Submitted by Biomedical Products Corp. (Beverly, US). The FDA issued a Cleared decision on November 18, 1999 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1155 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Biomedical Products Corp. devices

FDA 510(k) Submission Details - K992915

510(k) Number K992915 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 1999
Decision Date November 18, 1999
Days to Decision 80 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
8d faster than avg
Panel avg: 88d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JHI Device Classification - Class 2, Special Controls

Product Code JHI Visual, Pregnancy Hcg, Prescription Use
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1155
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - JHI Visual, Pregnancy Hcg, Prescription Use

All 274
Devices cleared under the same product code (JHI) and FDA review panel - the closest regulatory comparables to K992915.
CLEARVIEW EASY HCG PREGNANCY TEST
K993703 · Unipath , Ltd. · Dec 1999
ACON ONE STEP PREGNANCY TEST STRIP (URINE)
K993203 · ACON Laboratories, Inc. · Dec 1999
ACON HCG ONE STEP PREGNANCY TEST DEVICE (URINE)
K993317 · ACON Laboratories, Inc. · Dec 1999
INSURE PRO TEST
K992695 · Inbios Intl., Inc. · Oct 1999
ACON COMBO PREGNANCY
K993065 · ACON Laboratories, Inc. · Oct 1999
ACCUNATE-ONE STEP, ACCUNATE-ONE STEP CASSETTE
K992397 · Cenogenics Corp. · Aug 1999