Atlas FDA

MAPLESON D CIRCUIT

FDA 510(k) clearance K942570 · decided 1994-06-10

Clearance details

K-number
K942570
Device name
MAPLESON D CIRCUIT
Applicant
Med-Plastics Intl., Inc.
Decision
Substantially Equivalent
Date received
1994-05-31
Decision date
1994-06-10
Days to decision
10 days
Clearance type
Traditional
Product code
CAI
Device class
1
Regulation number
868.5240
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
CONDENSATE COLLECTION KIT (K954480)Nova-Ventrx1995-12-29
UNICOR, INC. GAS SAMPLING LINES & CONNECTORS (K953788)Unicor, Inc.1995-09-19
UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT (K953787)Unicor, Inc.1995-09-19
PRIMA ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS (K952014)Prima, Inc.1995-05-22
PRIMA ADULT GAS SAMPLING CIRCUITS (K952019)Prima, Inc.1995-05-22
PRIMA COAXIAL CIRCUITS (K952018)Prima, Inc.1995-05-22
PRIMA PEDIATRIC GAS SAMPLING CIRCUITS (K952016)Prima, Inc.1995-05-22
PRIMA MAPLESON D CIRCUIT (K952017)Prima, Inc.1995-05-22
PRIMA PEDIATRIC ANESTHESIA CIRCUITS (K952020)Prima, Inc.1995-05-22
PRIMA PEDIATRIC TEMPERATURE MONITORING CIRCUITS (K952009)Prima, Inc.1995-05-19
SPIRO-FLEX (K945565)Inhalation Plastics1995-01-13
NEONATAL BREATHING CIRCUIT MODIFICATION (K932288)Simplex Medical Systems, Inc.1994-12-30

Recalls involving this device

No recalls on record reference this clearance.