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FDA 510(k)

GLATTELAST COMPRESSION PANTY HOSE

K-Number: K841252 · 1984-06-27

Decision Date1984-06-27
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GLATTELAST COMPRESSION PANTY HOSE is the device name listed in this FDA 510(k) record. The listed applicant is Baurs Krey Assoc., Inc.. It received FDA 510(k) clearance on 1984-06-27 under 510(k) number K841252. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLATTELAST COMPRESSION PANTY HOSE?

GLATTELAST COMPRESSION PANTY HOSE is a medical device that received FDA 510(k) clearance on 1984-06-27. The listed applicant is Baurs Krey Assoc., Inc.. The 510(k) number is K841252.

When did GLATTELAST COMPRESSION PANTY HOSE receive FDA 510(k) clearance?

GLATTELAST COMPRESSION PANTY HOSE received FDA 510(k) clearance on 1984-06-27, under 510(k) number K841252.

Who is the listed applicant for GLATTELAST COMPRESSION PANTY HOSE?

The FDA 510(k) record lists Baurs Krey Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLATTELAST COMPRESSION PANTY HOSE?

The FDA product code for GLATTELAST COMPRESSION PANTY HOSE is DWL.

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 Baurs Krey Assoc., 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.

Related Devices (Code: DWL)

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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