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FDA 510(k)

S & W MODEL ASO

K-Number: K830873 · 1983-05-13

ApplicantS & W Enterprises, Inc.
Decision Date1983-05-13
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

S & W MODEL ASO is the device name listed in this FDA 510(k) record. The listed applicant is S & W Enterprises, Inc.. It received FDA 510(k) clearance on 1983-05-13 under 510(k) number K830873. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S & W MODEL ASO?

S & W MODEL ASO is a medical device that received FDA 510(k) clearance on 1983-05-13. The listed applicant is S & W Enterprises, Inc.. The 510(k) number is K830873.

When did S & W MODEL ASO receive FDA 510(k) clearance?

S & W MODEL ASO received FDA 510(k) clearance on 1983-05-13, under 510(k) number K830873.

Who is the listed applicant for S & W MODEL ASO?

The FDA 510(k) record lists S & W Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for S & W MODEL ASO?

The FDA product code for S & W MODEL ASO is KNC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing S & W Enterprises, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K864817S&W MODEL HIGH-LOW MAT TABLE, VARIOUS MODELSK841145TILT TABLE 53K832768S & W SW52E W/POWER BACK LIFTK830874S & W MODEL SW 37K830875S & W MODEL 29

Related Devices (Code: KNC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K001261L720 EXAMINATION CHAIRLuneau Gynecologie SAK932035NON-LINTING DELIVERY BLANKETAmsco Sterile Recoveries, Inc.K924420MEDICAL DISPOSABLE BEDDINGHill-Rom, Inc.K914544BD6000 THE OPTIMA & BD5000 BIRTHING BEDLic Care, Inc.K915779AFFINITY BED MODEL 3600 SERIESHill-Rom, Inc.K903973GARDOSI BIRTHING CUSHIONGraphic Controls Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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