Atlas FDA

MODEL 322 CLINICAL AUDIOMETER

FDA 510(k) clearance K930203 · decided 1993-07-08

Clearance details

K-number
K930203
Device name
MODEL 322 CLINICAL AUDIOMETER
Applicant
Virtual Corp.
Decision
Substantially Equivalent
Date received
1993-01-14
Decision date
1993-07-08
Days to decision
175 days
Clearance type
Traditional
Product code
EWD
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Portland, OR, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Virtual Corp.

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057 (K020296)Apothecary Products, Inc.2002-06-25
SUPER SILIPLUGS EAR PLUGS (K972923)Interview Medical Technology Corp.1997-10-27
SILICONE PUTTY EAR PLUGS (K971517)Bentec Medical, Inc.1997-06-02
HEARSAVER (K962292)Emtech Laboratories1996-10-29
THE VIRTUAL M-332 (K960500)Virtual Corp.1996-04-03
DOC'S PROPLUGS EAR PLUGS (K945376)Doc'S Proplugs, Inc.1995-11-14
#903 SILAFLEX II (K915739)Flents Products Co., Inc.1992-06-30
SEAL-RITE SILICONE EAR PLUG (K910177)Flents Products Co., Inc.1991-06-24
DOC'S PROPLUGS EAR PLUGS (K862045)Doc'S Proplugs, Inc.1987-04-10
MEDCO CUSTOM EAR PROTECTOR MOLD KIT (K821187)Santa Barbara Medco, Inc.1982-05-27
BILSOM PROPP (K791608)Bilson International, Inc.1979-10-10
EAR STOPPLES FOR NOISE ATTENTION (K781907)Crown Delta Corp.1978-11-22

Recalls involving this device

No recalls on record reference this clearance.