FDA 510(k)

SURGICARE MODEL 1000

K-Number: K822447 · 1982-10-18

ApplicantSurgicare Scientific Laboratory, Inc.

Decision Date1982-10-18

Product Code

DecisionSubstantially Equivalent

Device Summary

SURGICARE MODEL 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Surgicare Scientific Laboratory, Inc.. It received FDA 510(k) clearance on 1982-10-18 under 510(k) number K822447. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICARE MODEL 1000?

SURGICARE MODEL 1000 is a medical device that received FDA 510(k) clearance on 1982-10-18. The listed applicant is Surgicare Scientific Laboratory, Inc.. The 510(k) number is K822447.

When did SURGICARE MODEL 1000 receive FDA 510(k) clearance?

SURGICARE MODEL 1000 received FDA 510(k) clearance on 1982-10-18, under 510(k) number K822447.

Who is the listed applicant for SURGICARE MODEL 1000?

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

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 Surgicare Scientific Laboratory, Inc. as applicant

K823670E.S. PENCIL K822513MODEL #2000 HI-TEMP & #3000 LOW-TEMP

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.