Cleared Traditional

K770355 - PIPETTOR W/DETIPPER

K770355 is the FDA 510(k) clearance for PIPETTOR W/DETIPPER by Sherwood Medical Industries. It is a Class 1 Microbiology device (product code JQW) cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K770355 · Sherwood Medical Industries · Microbiology device
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Mar 1977
Decision
14d
Days
Class 1
Risk

K770355 is an FDA 510(k) clearance for the PIPETTOR W/DETIPPER. Classified as Station, Pipetting And Diluting, For Clinical Use (product code JQW), Class I - General Controls.

Submitted by Sherwood Medical Industries (Mchenry, US). The FDA issued a Cleared decision on March 8, 1977 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 862.2750 - the FDA microbiology 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 Industries devices

Submission Details

510(k) Number K770355 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 1977
Decision Date March 08, 1977
Days to Decision 14 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 102d · This submission: 14d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JQW Station, Pipetting And Diluting, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2750
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 - JQW Station, Pipetting And Diluting, For Clinical Use

All 63
Devices cleared under the same product code (JQW) and FDA review panel - the closest regulatory comparables to K770355.
ASPIRATOR, MANUEL
K780208 · Dade, Baxter Travenol Diagnostics, Inc. · Mar 1978
PIPETTE, DISPENSING, MODEL ADP-30SD
K770772 · G.D. Searle and Co. · Jul 1977
PIPETTE, DILUTING, MODEL ADP-30SD
K770773 · G.D. Searle and Co. · Jul 1977
ANALYTIX AUTO SAMPLE PREP. STA. 1600
K770210 · G.D. Searle and Co. · Feb 1977