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FDA 510(k)

PATIENT WARMER MODEL 100C

K-Number: K910915 · 1991-07-16

ApplicantDevelopmed Corp.
Decision Date1991-07-16
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT WARMER MODEL 100C is the device name listed in this FDA 510(k) record. The listed applicant is Developmed Corp.. It received FDA 510(k) clearance on 1991-07-16 under 510(k) number K910915. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT WARMER MODEL 100C?

PATIENT WARMER MODEL 100C is a medical device that received FDA 510(k) clearance on 1991-07-16. The listed applicant is Developmed Corp.. The 510(k) number is K910915.

When did PATIENT WARMER MODEL 100C receive FDA 510(k) clearance?

PATIENT WARMER MODEL 100C received FDA 510(k) clearance on 1991-07-16, under 510(k) number K910915.

Who is the listed applicant for PATIENT WARMER MODEL 100C?

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

What is the FDA product code for PATIENT WARMER MODEL 100C?

The FDA product code for PATIENT WARMER MODEL 100C is FMT.

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.

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Other records listing Developmed Corp. 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.

K871448MODEL 105 VENTILATOR

Related Devices (Code: FMT)

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.

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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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