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FDA 510(k)

2,2DIMETHOXY-2-PHENYLACETOPHENONE

K-Number: K771244 · 1977-09-12

ApplicantSolar Laboratories, Inc.
Decision Date1977-09-12
Product Code
DecisionSubstantially Equivalent

Device Summary

2,2DIMETHOXY-2-PHENYLACETOPHENONE is the device name listed in this FDA 510(k) record. The listed applicant is Solar Laboratories, Inc.. It received FDA 510(k) clearance on 1977-09-12 under 510(k) number K771244. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2,2DIMETHOXY-2-PHENYLACETOPHENONE?

2,2DIMETHOXY-2-PHENYLACETOPHENONE is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is Solar Laboratories, Inc.. The 510(k) number is K771244.

When did 2,2DIMETHOXY-2-PHENYLACETOPHENONE receive FDA 510(k) clearance?

2,2DIMETHOXY-2-PHENYLACETOPHENONE received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771244.

Who is the listed applicant for 2,2DIMETHOXY-2-PHENYLACETOPHENONE?

The FDA 510(k) record lists Solar Laboratories, 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 Solar Laboratories, 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.

K770134LIGHTCAST II STOCKINETTEK770133LIGHTCAST II CASTING SYSTEM (MODIFIED)K761222BENZOIN ISOBUTYL ETHERK760413TAPE, LIGHTCAST II WB

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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