Cleared Traditional

K812933 - LANCER SPECIMEN CONTAINER

K812933 is an FDA 510(k) clearance for LANCER SPECIMEN CONTAINER, manufactured by Sherwood Medical Co.. The device is a Class 1 General Hospital device with product code FMH cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K812933 · Sherwood Medical Co. · General Hospital
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Nov 1981
Decision
17d
Days
Class 1
Risk

K812933 is an FDA 510(k) clearance for the LANCER SPECIMEN CONTAINER. Classified as Container, Specimen, Sterile (product code FMH), Class I - General Controls.

Submitted by Sherwood Medical Co. (Mchenry, US). The FDA issued a Cleared decision on November 6, 1981 after a review of 17 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 864.3250 - the FDA general hospital 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 Sherwood Medical Co. devices

FDA 510(k) Submission Details - K812933

510(k) Number K812933 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 20, 1981
Decision Date November 06, 1981
Days to Decision 17 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
112d faster than avg
Panel avg: 129d · This submission: 17d
Pathway characteristics
Predicate-based equivalence.

FMH Device Classification - Class 1, General Controls

Product Code FMH Container, Specimen, Sterile
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.3250
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 - FMH Container, Specimen, Sterile

All 14
Devices cleared under the same product code (FMH) and FDA review panel - the closest regulatory comparables to K812933.
VARIOUS-SPECIMEN COLLECTORS
K823763 · Cordis Corp. · Jan 1983
SPECIMEN SET
K802340 · American Pharmaseal Div. Ahsc · Oct 1980
URINE SPECIMEN CONTAINER #'S 1013-1016
K802002 · Pollak (Intl.), Ltd. · Sep 1980
MIDSTREAM COLLECTION KIT
K800947 · Sage Products, Inc. · May 1980
ABCO MIDSTREAM URINE COLLECTION SET
K800233 · Abco Dealers, Inc. · Feb 1980
SPECIMEN COLLECTION PAN
K800309 · Sage Products, Inc. · Feb 1980