510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K951127Substantially Equivalent

Hewlett-Packard Model M1026a Anesthetic Gas Module

Hewlett-Packard Co., 71004 Boblingen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951127 is the FDA 510(k) clearance record for HEWLETT-PACKARD MODEL M1026A ANESTHETIC GAS MODULE, a class II device, cleared for Hewlett-Packard GmbH on under FDA product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). FDA records list 246 510(k) clearances for Hewlett-Packard GmbH, from to . As of , FDA records show no recalls naming K951127.

Clearance record

Decision date
Received
(11 days to decision)
Product code
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Regulation
21 CFR 868.1400
Device class
Class II
Review panel
Anesthesiology
Applicant
Hewlett-Packard GmbH Medizinelektronik, 71004 Boblingen, DE
510(k) summary
Summary
Third party review
No

Clearances, product code CCK

Trailing 12 months
3 clearances under product code CCK in the twelve months to November 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CCK, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20261
August 20261
September 20260
October 20260
November 20260