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FDA 510(k)

SUR FLO THERMAL THERAPY PADS

K-Number: K930634 · 1993-11-01

Decision Date1993-11-01
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUR FLO THERMAL THERAPY PADS is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1993-11-01 under 510(k) number K930634. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUR FLO THERMAL THERAPY PADS?

SUR FLO THERMAL THERAPY PADS is a medical device that received FDA 510(k) clearance on 1993-11-01. The listed applicant is Buckman Co., Inc.. The 510(k) number is K930634.

When did SUR FLO THERMAL THERAPY PADS receive FDA 510(k) clearance?

SUR FLO THERMAL THERAPY PADS received FDA 510(k) clearance on 1993-11-01, under 510(k) number K930634.

Who is the listed applicant for SUR FLO THERMAL THERAPY PADS?

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

What is the FDA product code for SUR FLO THERMAL THERAPY PADS?

The FDA product code for SUR FLO THERMAL THERAPY PADS is ILO.

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 Buckman Co., 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 111 devices →

Related Devices (Code: ILO)

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

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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