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FDA 510(k)

MEGABED 1000

K-Number: K872925 · 1987-09-15

ApplicantSurgi-Med, Inc.
Decision Date1987-09-15
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEGABED 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Surgi-Med, Inc.. It received FDA 510(k) clearance on 1987-09-15 under 510(k) number K872925. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEGABED 1000?

MEGABED 1000 is a medical device that received FDA 510(k) clearance on 1987-09-15. The listed applicant is Surgi-Med, Inc.. The 510(k) number is K872925.

When did MEGABED 1000 receive FDA 510(k) clearance?

MEGABED 1000 received FDA 510(k) clearance on 1987-09-15, under 510(k) number K872925.

Who is the listed applicant for MEGABED 1000?

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

What is the FDA product code for MEGABED 1000?

The FDA product code for MEGABED 1000 is FNL.

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Other records listing Surgi-Med, 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.

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Related Devices (Code: FNL)

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

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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