Atlas FDA

ULTIMATE SEAL

FDA 510(k) clearance K960401 · decided 1996-06-20

Clearance details

K-number
K960401
Device name
ULTIMATE SEAL
Applicant
Hans Rudolph, Inc.
Decision
Substantially Equivalent
Date received
1996-01-29
Decision date
1996-06-20
Days to decision
143 days
Clearance type
Traditional
Product code
KGB
Device class
1
Regulation number
868.5570
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Kansas City, MO, 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
POCKET RESCUE (K970688)Cheen Houng Ent. Co. , Ltd.1997-09-26
COMBO MASK (K941336)Gam Industries, Inc.1994-09-09
CHALLENGE POWDER-FREE, HYPOALLERGENIC, SYNTHETIC SURGICAL GLOVES (K935917)Bd Becton Dickinson Vacutainer Systems Preanalytic1994-02-04
COMPACT MASK (K932347)Vital Signs, Inc.1994-01-10
NONREBREATHING VALVE (K933583)Hans Rudolph, Inc.1994-01-03
LAERDAL(TM) POCKET MASK, MODIFICATION (K933048)Laerdal Medical Corp.1993-12-02
PROFAST(R)-DENTURE ADHESIVE CREAM (K930336)Fittydent-Altwirth & Schmitt GmbH1993-08-24
NON REBREATHING MASK (K913164)Specialty Packaging Producs, Inc.1992-01-15
MOUTH-TO-MASK VENTILATORY ADJUNCT (K883766)Medic One1988-10-21
OXYGEN MASK, CONCENTRATION AEROSOL MASK (K790162)Airlife, Inc.1979-04-20
OXYGEN MASK W/RESERVOIR BAG (K790161)Airlife, Inc.1979-04-20
MASK, OXYGEN, NONBREATHING (K781414)Vitalab Products Corp.1978-09-07

Recalls involving this device

No recalls on record reference this clearance.