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FDA 510(k)

SILKAIR LOW AIRLOSS THERAPY

K-Number: K964873 · 1997-07-03

Decision Date1997-07-03
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SILKAIR LOW AIRLOSS THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom, Inc.. It received FDA 510(k) clearance on 1997-07-03 under 510(k) number K964873. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILKAIR LOW AIRLOSS THERAPY?

SILKAIR LOW AIRLOSS THERAPY is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K964873.

When did SILKAIR LOW AIRLOSS THERAPY receive FDA 510(k) clearance?

SILKAIR LOW AIRLOSS THERAPY received FDA 510(k) clearance on 1997-07-03, under 510(k) number K964873.

Who is the listed applicant for SILKAIR LOW AIRLOSS THERAPY?

The FDA 510(k) record lists Hill-Rom, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILKAIR LOW AIRLOSS THERAPY?

The FDA product code for SILKAIR LOW AIRLOSS THERAPY is IOQ.

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.

Other records listing Hill-Rom, 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.

View all 34 devices →

Related Devices (Code: IOQ)

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.

Official Source

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

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