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FDA 510(k)

INSTRUMENT WARMER

K-Number: K925530 · 1993-06-18

ApplicantSuperior Healthcare Group, Inc.
Decision Date1993-06-18
Product CodeFMS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Superior Healthcare Group, Inc.. It received FDA 510(k) clearance on 1993-06-18 under 510(k) number K925530. The device is classified under product code FMS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT WARMER?

INSTRUMENT WARMER is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Superior Healthcare Group, Inc.. The 510(k) number is K925530.

When did INSTRUMENT WARMER receive FDA 510(k) clearance?

INSTRUMENT WARMER received FDA 510(k) clearance on 1993-06-18, under 510(k) number K925530.

Who is the listed applicant for INSTRUMENT WARMER?

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

What is the FDA product code for INSTRUMENT WARMER?

The FDA product code for INSTRUMENT WARMER is FMS.

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Other records listing Superior Healthcare Group, 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.

K924764OVERTUBE FOR ENDSCOPIC LIGATORK905755NON-STERILE PATIENT EXAMINATION GLOVESK903347SODIUM CHLORIDE SOLUTIONK904216STERILE WATER SOLUTION CATALOG # 10000K903340STERILE URETHRAL CATHETER PROCEDURE KITSK896321NO. 34100 - 8 FR & NO. 34400 - 14 FR CLOSED TRACH.

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Related Devices (Code: FMS)

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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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