Atlas FDA

SHELL KRATON THERMO-PLASTIC RUBBER COMP.

FDA 510(k) clearance K803069 · decided 1980-12-22

Clearance details

K-number
K803069
Device name
SHELL KRATON THERMO-PLASTIC RUBBER COMP.
Applicant
Warren E. Collins, Inc.
Decision
Substantially Equivalent
Date received
1980-12-05
Decision date
1980-12-22
Days to decision
17 days
Clearance type
Traditional
Product code
BYP
Device class
1
Regulation number
868.5620
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Walker, MI, 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
NORTH STATE PLASTICS RESPIRATORY MOUTHPIECE (K955657)North State Plastics, Inc.1996-03-12
TRUZONE PFM DISPOSABLE MOUTHPIECE (K944512)Monaghan Medical Corp.1994-11-02
BREATHING MOUTHPIECE (K893791)Diemolding Corp.1989-06-23
AEROCHAMBER (K872037)Monaghan Medical Corp.1987-07-24
SAFE-T-SHIELD MOUTHPIECE (K865093)Medi Nuclear Corp., Inc.1987-01-15
INHALATION AID (K863049)Boehringer Ingelheim Pharmaceuticals, Inc.1986-10-15
MP-4400 MOUTHPIECE-FLANGE SEAL (K862788)Medipart Jerry Alexander1986-08-01
PLASTIC MOUTH BARRIER HSV-I (K853266)Westmark Enterprises, Inc.1985-10-29
MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410 (K853572)Medipart Jerry Alexander1985-10-29
MEDIPART DISPOS. MOUTHPIECE W/22MM O.D. MP-4411 (K853574)Medipart Jerry Alexander1985-10-29
MEDIPART MOUTHPIECE MP-1010 (K853575)Medipart Jerry Alexander1985-10-29
E-Z-GUARD MOUTHPIECE (K853402)E-Z-Em, Inc.1985-10-23

Recalls involving this device

No recalls on record reference this clearance.