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FDA 510(k)

SELF-CONTAINED SURGICAL SLUSH FREEZER

K-Number: K913777 · 1991-09-25

ApplicantTaylor Corp.
Decision Date1991-09-25
Product CodeJRM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SELF-CONTAINED SURGICAL SLUSH FREEZER is the device name listed in this FDA 510(k) record. The listed applicant is Taylor Corp.. It received FDA 510(k) clearance on 1991-09-25 under 510(k) number K913777. The device is classified under product code JRM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELF-CONTAINED SURGICAL SLUSH FREEZER?

SELF-CONTAINED SURGICAL SLUSH FREEZER is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is Taylor Corp.. The 510(k) number is K913777.

When did SELF-CONTAINED SURGICAL SLUSH FREEZER receive FDA 510(k) clearance?

SELF-CONTAINED SURGICAL SLUSH FREEZER received FDA 510(k) clearance on 1991-09-25, under 510(k) number K913777.

Who is the listed applicant for SELF-CONTAINED SURGICAL SLUSH FREEZER?

The FDA 510(k) record lists Taylor Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SELF-CONTAINED SURGICAL SLUSH FREEZER?

The FDA product code for SELF-CONTAINED SURGICAL SLUSH FREEZER is JRM.

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Related Devices (Code: JRM)

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.

K921569ORS-200Mnlase, Inc.K921570ORS-300Mnlase, Inc.K921568ORS-100Mnlase, Inc.K915427ORS-1000Mnlase, Inc.K894006SANISERV SURGICAL SLUSH SYSTEMSaniserv, Inc.K782077LANCER ICE CUBESherwood Medical Industries

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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