Cleared Traditional

K891044 - LASER SPECULA

K891044 is the FDA 510(k) clearance for LASER SPECULA by Zinnanti Surgical Instruments, Inc.. It is a Class 1 Obstetrics & Gynecology device (product code HDF) cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K891044 · Zinnanti Surgical Instruments, Inc. · Obstetrics & Gynecology device
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Mar 1989
Decision
17d
Days
Class 1
Risk

K891044 is an FDA 510(k) clearance for the LASER SPECULA. Classified as Speculum, Vaginal, Metal (product code HDF), Class I - General Controls.

Submitted by Zinnanti Surgical Instruments, Inc. (Chatsworth, US). The FDA issued a Cleared decision on March 17, 1989 after a review of 17 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.4520 - the FDA obstetrics and gynecology device 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 Zinnanti Surgical Instruments, Inc. devices

Submission Details

510(k) Number K891044 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 28, 1989
Decision Date March 17, 1989
Days to Decision 17 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
143d faster than avg
Panel avg: 160d · This submission: 17d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HDF Speculum, Vaginal, Metal
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 884.4520
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - HDF Speculum, Vaginal, Metal

All 8
Devices cleared under the same product code (HDF) and FDA review panel - the closest regulatory comparables to K891044.
VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT
K926429 · Thomasville Medical Assoc. · Feb 1994
MIYA SPECULUM
K891041 · Zinnanti Surgical Instruments, Inc. · Mar 1989
VAGINAL SPECULUM
K890375 · Kinetic Medical Products · Feb 1989
WELLINGTON HOSPITAL PATTERN SELF RETAINING VAGINAL
K853640 · Downs Surgical , Ltd. · Oct 1985
61-100 TO 61-124 VARIOUS VAGINAL SPECVIA(CUSCO,GRA
K851799 · Artiberia · May 1985
WELLINGTON HOSPITAL PATTERN SELF-RETAIN
K843388 · Downs Surgical , Ltd. · Oct 1984